Canonical Allele Identifier: CA367398973
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs754337045
gnomAD v4: 7-44145645-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145645G>T , CM000669.2:g.44145645G>T GRCh38
NC_000007.13:g.44185244G>T , CM000669.1:g.44185244G>T GRCh37
NC_000007.12:g.44151769G>T NCBI36
NG_008847.1:g.48779C>A
NG_008847.2:g.57526C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*1103C>A ENSP00000379142.4:n.*1103C>A
ENST00000616242.5:c.*225C>A ENSP00000482149.2:n.*225C>A
ENST00000683378.1:n.331C>A
ENST00000336642.9:c.139C>A ENSP00000338009.5:p.Arg47Ser
ENST00000345378.7:c.1108C>A ENSP00000223366.2:p.Arg370Ser
ENST00000403799.8:c.1105C>A MANE Select ENSP00000384247.3:p.Arg369Ser
ENST00000671824.1:c.1168C>A ENSP00000500264.1:p.Arg390Ser
ENST00000672743.1:n.117C>A
ENST00000673284.1:c.1105C>A ENSP00000499852.1:p.Arg369Ser
ENST00000336642.8:c.157C>A ENSP00000338009.4:p.Arg53Ser
ENST00000345378.6:c.1108C>A ENSP00000223366.2:p.Arg370Ser
ENST00000395796.7:c.1102C>A ENSP00000379142.3:p.Arg368Ser
ENST00000403799.7:c.1105C>A ENSP00000384247.3:p.Arg369Ser
ENST00000437084.1:c.1054C>A ENSP00000402840.1:p.Arg352Ser
ENST00000459642.1:n.485C>A
ENST00000473353.1:n.403C>A
ENST00000616242.4:c.1102C>A ENSP00000482149.1:p.Arg368Ser
NM_000162.3:c.1105C>A NP_000153.1:p.Arg369Ser
NM_033507.1:c.1108C>A NP_277042.1:p.Arg370Ser
NM_033508.1:c.1102C>A NP_277043.1:p.Arg368Ser
NM_000162.4:c.1105C>A NP_000153.1:p.Arg369Ser
NM_001354800.1:c.1105C>A NP_001341729.1:p.Arg369Ser
NM_001354801.1:c.94C>A NP_001341730.1:p.Arg32Ser
NM_001354802.1:c.-36C>A NP_001341731.1:n.-36C>A
NM_001354803.1:c.139C>A NP_001341732.1:p.Arg47Ser
NM_033507.2:c.1108C>A NP_277042.1:p.Arg370Ser
NM_033508.2:c.1102C>A NP_277043.1:p.Arg368Ser
XM_024446707.1:c.-36C>A XP_024302475.1:n.-36C>A
NM_000162.5:c.1105C>A MANE Select NP_000153.1:p.Arg369Ser
NM_033507.3:c.1108C>A NP_277042.1:p.Arg370Ser
NM_033508.3:c.1102C>A NP_277043.1:p.Arg368Ser
NM_001354803.2:c.139C>A NP_001341732.1:p.Arg47Ser