Canonical Allele Identifier: CA651288862
Gene: GCK HGNC NCBI

Linked Data

COSMIC: COSN26786686
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147455G>A , CM000669.2:g.44147455G>A GRCh38
NC_000007.13:g.44187054G>A , CM000669.1:g.44187054G>A GRCh37
NC_000007.12:g.44153579G>A NCBI36
NG_008847.1:g.46969C>T
NG_008847.2:g.55716C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*861+195C>T ENSP00000379142.4:n.*861+195C>T
ENST00000616242.5:c.853+205C>T ENSP00000482149.2:n.853+205C>T
ENST00000345378.7:c.866+195C>T ENSP00000223366.2:n.866+195C>T
ENST00000403799.8:c.863+195C>T MANE Select ENSP00000384247.3:n.863+195C>T
ENST00000671824.1:c.854-42C>T ENSP00000500264.1:n.854-42C>T
ENST00000673284.1:c.863+195C>T ENSP00000499852.1:n.863+195C>T
ENST00000345378.6:c.866+195C>T ENSP00000223366.2:n.866+195C>T
ENST00000395796.7:c.860+195C>T ENSP00000379142.3:n.860+195C>T
ENST00000403799.7:c.863+195C>T ENSP00000384247.3:n.863+195C>T
ENST00000437084.1:c.812+195C>T ENSP00000402840.1:n.812+195C>T
ENST00000616242.4:c.860+195C>T ENSP00000482149.1:n.860+195C>T
NM_000162.3:c.863+195C>T NP_000153.1:n.863+195C>T
NM_033507.1:c.866+195C>T NP_277042.1:n.866+195C>T
NM_033508.1:c.860+195C>T NP_277043.1:n.860+195C>T
NM_000162.4:c.863+195C>T NP_000153.1:n.863+195C>T
NM_001354800.1:c.863+195C>T NP_001341729.1:n.863+195C>T
NM_033507.2:c.866+195C>T NP_277042.1:n.866+195C>T
NM_033508.2:c.860+195C>T NP_277043.1:n.860+195C>T
NM_000162.5:c.863+195C>T MANE Select NP_000153.1:n.863+195C>T
NM_033507.3:c.866+195C>T NP_277042.1:n.866+195C>T
NM_033508.3:c.860+195C>T NP_277043.1:n.860+195C>T
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