Canonical Allele Identifier: CA367398204
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs2096271210
gnomAD v4: 7-44145500-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145500G>C , CM000669.2:g.44145500G>C GRCh38
NC_000007.13:g.44185099G>C , CM000669.1:g.44185099G>C GRCh37
NC_000007.12:g.44151624G>C NCBI36
NG_008847.1:g.48924C>G
NG_008847.2:g.57671C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1248C>G ENSP00000379142.4:n.*1248C>G
ENST00000616242.5:c.*370C>G ENSP00000482149.2:n.*370C>G
ENST00000683378.1:n.476C>G
ENST00000336642.9:c.284C>G ENSP00000338009.5:p.Pro95Arg
ENST00000345378.7:c.1253C>G ENSP00000223366.2:p.Pro418Arg
ENST00000403799.8:c.1250C>G MANE Select ENSP00000384247.3:p.Pro417Arg
ENST00000671824.1:c.1313C>G ENSP00000500264.1:p.Pro438Arg
ENST00000672743.1:n.262C>G
ENST00000673284.1:c.1250C>G ENSP00000499852.1:p.Pro417Arg
ENST00000336642.8:c.302C>G ENSP00000338009.4:p.Pro101Arg
ENST00000345378.6:c.1253C>G ENSP00000223366.2:p.Pro418Arg
ENST00000395796.7:c.1247C>G ENSP00000379142.3:p.Pro416Arg
ENST00000403799.7:c.1250C>G ENSP00000384247.3:p.Pro417Arg
ENST00000437084.1:c.1199C>G ENSP00000402840.1:p.Pro400Arg
ENST00000459642.1:n.630C>G
ENST00000616242.4:c.1247C>G ENSP00000482149.1:p.Pro416Arg
NM_000162.3:c.1250C>G NP_000153.1:p.Pro417Arg
NM_033507.1:c.1253C>G NP_277042.1:p.Pro418Arg
NM_033508.1:c.1247C>G NP_277043.1:p.Pro416Arg
NM_000162.4:c.1250C>G NP_000153.1:p.Pro417Arg
NM_001354800.1:c.1250C>G NP_001341729.1:p.Pro417Arg
NM_001354801.1:c.239C>G NP_001341730.1:p.Pro80Arg
NM_001354802.1:c.110C>G NP_001341731.1:p.Pro37Arg
NM_001354803.1:c.284C>G NP_001341732.1:p.Pro95Arg
NM_033507.2:c.1253C>G NP_277042.1:p.Pro418Arg
NM_033508.2:c.1247C>G NP_277043.1:p.Pro416Arg
XM_024446707.1:c.110C>G XP_024302475.1:p.Pro37Arg
NM_000162.5:c.1250C>G MANE Select NP_000153.1:p.Pro417Arg
NM_033507.3:c.1253C>G NP_277042.1:p.Pro418Arg
NM_033508.3:c.1247C>G NP_277043.1:p.Pro416Arg
NM_001354803.2:c.284C>G NP_001341732.1:p.Pro95Arg