Canonical Allele Identifier: CA2682579255
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44144899-T-TGCTGATTGGGGGCCAGGCC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144899_44144900insGCTGATTGGGGGCCAGGCC , CM000669.2:g.44144899_44144900insGCTGATTGGGGGCCAGGCC GRCh38
NC_000007.13:g.44184498_44184499insGCTGATTGGGGGCCAGGCC , CM000669.1:g.44184498_44184499insGCTGATTGGGGGCCAGGCC GRCh37
NC_000007.12:g.44151023_44151024insGCTGATTGGGGGCCAGGCC NCBI36
NG_008847.1:g.49524_49525insGGCCTGGCCCCCAATCAGC
NG_008847.2:g.58271_58272insGGCCTGGCCCCCAATCAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1632_*1633insGGCCTGGCCCCCAATCAGC ENSP00000379142.4:n.*1632_*1633insGGCCTGGCCCCCAATCAGC
ENST00000616242.5:c.*754_*755insGGCCTGGCCCCCAATCAGC ENSP00000482149.2:n.*754_*755insGGCCTGGCCCCCAATCAGC
ENST00000683378.1:n.860_861insGGCCTGGCCCCCAATCAGC
ENST00000336642.9:c.*236_*237insGGCCTGGCCCCCAATCAGC ENSP00000338009.5:n.*236_*237insGGCCTGGCCCCCAATCAGC
ENST00000345378.7:c.*236_*237insGGCCTGGCCCCCAATCAGC ENSP00000223366.2:n.*236_*237insGGCCTGGCCCCCAATCAGC
ENST00000403799.8:c.*236_*237insGGCCTGGCCCCCAATCAGC MANE Select ENSP00000384247.3:n.*236_*237insGGCCTGGCCCCCAATCAGC
ENST00000671824.1:c.*236_*237insGGCCTGGCCCCCAATCAGC ENSP00000500264.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
ENST00000672743.1:n.381+265_381+266insGGCCTGGCCCCCAATCAGC
ENST00000673284.1:c.1369+265_1369+266insGGCCTGGCCCCCAATCAGC ENSP00000499852.1:n.1369+265_1369+266insGGCCTGGCCCCCAATCAGC
ENST00000336642.8:c.686_687insGGCCTGGCCCCCAATCAGC ENSP00000338009.4:n.686_687insGGCCTGGCCCCCAATCAGC
ENST00000345378.6:c.*236_*237insGGCCTGGCCCCCAATCAGC ENSP00000223366.2:n.*236_*237insGGCCTGGCCCCCAATCAGC
ENST00000395796.7:c.*236_*237insGGCCTGGCCCCCAATCAGC ENSP00000379142.3:n.*236_*237insGGCCTGGCCCCCAATCAGC
ENST00000403799.7:c.*236_*237insGGCCTGGCCCCCAATCAGC ENSP00000384247.3:n.*236_*237insGGCCTGGCCCCCAATCAGC
ENST00000459642.1:n.1014_1015insGGCCTGGCCCCCAATCAGC
ENST00000616242.4:c.1631_1632insGGCCTGGCCCCCAATCAGC ENSP00000482149.1:n.1631_1632insGGCCTGGCCCCCAATCAGC
NM_000162.3:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_000153.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_033507.1:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_277042.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_033508.1:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_277043.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_000162.4:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_000153.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_001354800.1:c.1369+265_1369+266insGGCCTGGCCCCCAATCAGC NP_001341729.1:n.1369+265_1369+266insGGCCTGGCCCCCAATCAGC
NM_001354801.1:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_001341730.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_001354802.1:c.229+265_229+266insGGCCTGGCCCCCAATCAGC NP_001341731.1:n.229+265_229+266insGGCCTGGCCCCCAATCAGC
NM_001354803.1:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_001341732.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_033507.2:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_277042.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_033508.2:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_277043.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
XM_024446707.1:c.*236_*237insGGCCTGGCCCCCAATCAGC XP_024302475.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_000162.5:c.*236_*237insGGCCTGGCCCCCAATCAGC MANE Select NP_000153.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_033507.3:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_277042.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_033508.3:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_277043.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
NM_001354803.2:c.*236_*237insGGCCTGGCCCCCAATCAGC NP_001341732.1:n.*236_*237insGGCCTGGCCCCCAATCAGC
Search 100 bp 5'
Search 100 bp 3'