Canonical Allele Identifier: CA367396755
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145148C>G , CM000669.2:g.44145148C>G GRCh38
NC_000007.13:g.44184747C>G , CM000669.1:g.44184747C>G GRCh37
NC_000007.12:g.44151272C>G NCBI36
NG_008847.1:g.49276G>C
NG_008847.2:g.58023G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1384G>C ENSP00000379142.4:n.*1384G>C
ENST00000616242.5:c.*506G>C ENSP00000482149.2:n.*506G>C
ENST00000683378.1:n.612G>C
ENST00000336642.9:c.420G>C ENSP00000338009.5:p.Met140Ile
ENST00000345378.7:c.1389G>C ENSP00000223366.2:p.Met463Ile
ENST00000403799.8:c.1386G>C MANE Select ENSP00000384247.3:p.Met462Ile
ENST00000671824.1:c.1449G>C ENSP00000500264.1:p.Met483Ile
ENST00000672743.1:n.381+17G>C
ENST00000673284.1:c.1369+17G>C ENSP00000499852.1:n.1369+17G>C
ENST00000336642.8:c.438G>C ENSP00000338009.4:p.Met146Ile
ENST00000345378.6:c.1389G>C ENSP00000223366.2:p.Met463Ile
ENST00000395796.7:c.1383G>C ENSP00000379142.3:p.Met461Ile
ENST00000403799.7:c.1386G>C ENSP00000384247.3:p.Met462Ile
ENST00000437084.1:c.1335G>C ENSP00000402840.1:p.Met445Ile
ENST00000459642.1:n.766G>C
ENST00000616242.4:c.1383G>C ENSP00000482149.1:p.Met461Ile
NM_000162.3:c.1386G>C NP_000153.1:p.Met462Ile
NM_033507.1:c.1389G>C NP_277042.1:p.Met463Ile
NM_033508.1:c.1383G>C NP_277043.1:p.Met461Ile
NM_000162.4:c.1386G>C NP_000153.1:p.Met462Ile
NM_001354800.1:c.1369+17G>C NP_001341729.1:n.1369+17G>C
NM_001354801.1:c.375G>C NP_001341730.1:p.Met125Ile
NM_001354802.1:c.229+17G>C NP_001341731.1:n.229+17G>C
NM_001354803.1:c.420G>C NP_001341732.1:p.Met140Ile
NM_033507.2:c.1389G>C NP_277042.1:p.Met463Ile
NM_033508.2:c.1383G>C NP_277043.1:p.Met461Ile
XM_024446707.1:c.246G>C XP_024302475.1:p.Met82Ile
NM_000162.5:c.1386G>C MANE Select NP_000153.1:p.Met462Ile
NM_033507.3:c.1389G>C NP_277042.1:p.Met463Ile
NM_033508.3:c.1383G>C NP_277043.1:p.Met461Ile
NM_001354803.2:c.420G>C NP_001341732.1:p.Met140Ile