Canonical Allele Identifier: CA454863063
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44145676-T-C
MyVariant Identifiers: chr7:g.44185275T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145676T>C , CM000669.2:g.44145676T>C GRCh38
NC_000007.13:g.44185275T>C , CM000669.1:g.44185275T>C GRCh37
NC_000007.12:g.44151800T>C NCBI36
NG_008847.1:g.48748A>G
NG_008847.2:g.57495A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1072A>G ENSP00000379142.4:n.*1072A>G
ENST00000616242.5:c.*194A>G ENSP00000482149.2:n.*194A>G
ENST00000683378.1:n.300A>G
ENST00000336642.9:c.108A>G ENSP00000338009.5:p.Arg36=
ENST00000345378.7:c.1077A>G ENSP00000223366.2:p.Arg359=
ENST00000403799.8:c.1074A>G MANE Select ENSP00000384247.3:p.Arg358=
ENST00000671824.1:c.1137A>G ENSP00000500264.1:p.Arg379=
ENST00000672743.1:n.86A>G
ENST00000673284.1:c.1074A>G ENSP00000499852.1:p.Arg358=
ENST00000336642.8:c.126A>G ENSP00000338009.4:p.Arg42=
ENST00000345378.6:c.1077A>G ENSP00000223366.2:p.Arg359=
ENST00000395796.7:c.1071A>G ENSP00000379142.3:p.Arg357=
ENST00000403799.7:c.1074A>G ENSP00000384247.3:p.Arg358=
ENST00000437084.1:c.1023A>G ENSP00000402840.1:p.Arg341=
ENST00000459642.1:n.454A>G
ENST00000473353.1:n.372A>G
ENST00000616242.4:c.1071A>G ENSP00000482149.1:p.Arg357=
NM_000162.3:c.1074A>G NP_000153.1:p.Arg358=
NM_033507.1:c.1077A>G NP_277042.1:p.Arg359=
NM_033508.1:c.1071A>G NP_277043.1:p.Arg357=
NM_000162.4:c.1074A>G NP_000153.1:p.Arg358=
NM_001354800.1:c.1074A>G NP_001341729.1:p.Arg358=
NM_001354801.1:c.63A>G NP_001341730.1:p.Arg21=
NM_001354802.1:c.-67A>G NP_001341731.1:n.-67A>G
NM_001354803.1:c.108A>G NP_001341732.1:p.Arg36=
NM_033507.2:c.1077A>G NP_277042.1:p.Arg359=
NM_033508.2:c.1071A>G NP_277043.1:p.Arg357=
XM_024446707.1:c.-67A>G XP_024302475.1:n.-67A>G
NM_000162.5:c.1074A>G MANE Select NP_000153.1:p.Arg358=
NM_033507.3:c.1077A>G NP_277042.1:p.Arg359=
NM_033508.3:c.1071A>G NP_277043.1:p.Arg357=
NM_001354803.2:c.108A>G NP_001341732.1:p.Arg36=