Canonical Allele Identifier: CA2682582183
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44145769-G-GGAGCGACA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145769_44145770insGAGCGACA , CM000669.2:g.44145769_44145770insGAGCGACA GRCh38
NC_000007.13:g.44185368_44185369insGAGCGACA , CM000669.1:g.44185368_44185369insGAGCGACA GRCh37
NC_000007.12:g.44151893_44151894insGAGCGACA NCBI36
NG_008847.1:g.48654_48655insTGTCGCTC
NG_008847.2:g.57401_57402insTGTCGCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1018-40_*1018-39insTGTCGCTC ENSP00000379142.4:n.*1018-40_*1018-39insTGTCGCTC
ENST00000616242.5:c.*140-40_*140-39insTGTCGCTC ENSP00000482149.2:n.*140-40_*140-39insTGTCGCTC
ENST00000683378.1:n.246-40_246-39insTGTCGCTC
ENST00000336642.9:c.54-40_54-39insTGTCGCTC ENSP00000338009.5:n.54-40_54-39insTGTCGCTC
ENST00000345378.7:c.1023-40_1023-39insTGTCGCTC ENSP00000223366.2:n.1023-40_1023-39insTGTCGCTC
ENST00000403799.8:c.1020-40_1020-39insTGTCGCTC MANE Select ENSP00000384247.3:n.1020-40_1020-39insTGTCGCTC
ENST00000671824.1:c.1083-40_1083-39insTGTCGCTC ENSP00000500264.1:n.1083-40_1083-39insTGTCGCTC
ENST00000672743.1:n.32-40_32-39insTGTCGCTC
ENST00000673284.1:c.1020-40_1020-39insTGTCGCTC ENSP00000499852.1:n.1020-40_1020-39insTGTCGCTC
ENST00000336642.8:c.72-40_72-39insTGTCGCTC ENSP00000338009.4:n.72-40_72-39insTGTCGCTC
ENST00000345378.6:c.1023-40_1023-39insTGTCGCTC ENSP00000223366.2:n.1023-40_1023-39insTGTCGCTC
ENST00000395796.7:c.1017-40_1017-39insTGTCGCTC ENSP00000379142.3:n.1017-40_1017-39insTGTCGCTC
ENST00000403799.7:c.1020-40_1020-39insTGTCGCTC ENSP00000384247.3:n.1020-40_1020-39insTGTCGCTC
ENST00000437084.1:c.969-40_969-39insTGTCGCTC ENSP00000402840.1:n.969-40_969-39insTGTCGCTC
ENST00000459642.1:n.360_361insTGTCGCTC
ENST00000473353.1:n.318-40_318-39insTGTCGCTC
ENST00000616242.4:c.1017-40_1017-39insTGTCGCTC ENSP00000482149.1:n.1017-40_1017-39insTGTCGCTC
NM_000162.3:c.1020-40_1020-39insTGTCGCTC NP_000153.1:n.1020-40_1020-39insTGTCGCTC
NM_033507.1:c.1023-40_1023-39insTGTCGCTC NP_277042.1:n.1023-40_1023-39insTGTCGCTC
NM_033508.1:c.1017-40_1017-39insTGTCGCTC NP_277043.1:n.1017-40_1017-39insTGTCGCTC
NM_000162.4:c.1020-40_1020-39insTGTCGCTC NP_000153.1:n.1020-40_1020-39insTGTCGCTC
NM_001354800.1:c.1020-40_1020-39insTGTCGCTC NP_001341729.1:n.1020-40_1020-39insTGTCGCTC
NM_001354801.1:c.9-40_9-39insTGTCGCTC NP_001341730.1:n.9-40_9-39insTGTCGCTC
NM_001354802.1:c.-121-40_-121-39insTGTCGCTC NP_001341731.1:n.-121-40_-121-39insTGTCGCTC
NM_001354803.1:c.54-40_54-39insTGTCGCTC NP_001341732.1:n.54-40_54-39insTGTCGCTC
NM_033507.2:c.1023-40_1023-39insTGTCGCTC NP_277042.1:n.1023-40_1023-39insTGTCGCTC
NM_033508.2:c.1017-40_1017-39insTGTCGCTC NP_277043.1:n.1017-40_1017-39insTGTCGCTC
XM_024446707.1:c.-121-40_-121-39insTGTCGCTC XP_024302475.1:n.-121-40_-121-39insTGTCGCTC
NM_000162.5:c.1020-40_1020-39insTGTCGCTC MANE Select NP_000153.1:n.1020-40_1020-39insTGTCGCTC
NM_033507.3:c.1023-40_1023-39insTGTCGCTC NP_277042.1:n.1023-40_1023-39insTGTCGCTC
NM_033508.3:c.1017-40_1017-39insTGTCGCTC NP_277043.1:n.1017-40_1017-39insTGTCGCTC
NM_001354803.2:c.54-40_54-39insTGTCGCTC NP_001341732.1:n.54-40_54-39insTGTCGCTC
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