Canonical Allele Identifier: CA2682589272

Gene: GCK

Linked Data

• gnomAD v4: 7-44147841-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147841G>A , CM000669.2:g.44147841G>A	GRCh38
NC_000007.13:g.44187440G>A , CM000669.1:g.44187440G>A	GRCh37
NC_000007.12:g.44153965G>A	NCBI36
NG_008847.1:g.46583C>T
NG_008847.2:g.55330C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*678-8C>T	ENSP00000379142.4:n.*678-8C>T
ENST00000616242.5:c.680-8C>T	ENSP00000482149.2:n.680-8C>T
ENST00000345378.7:c.683-8C>T	ENSP00000223366.2:n.683-8C>T
ENST00000403799.8:c.680-8C>T MANE Select	ENSP00000384247.3:n.680-8C>T
ENST00000671824.1:c.680-8C>T	ENSP00000500264.1:n.680-8C>T
ENST00000673284.1:c.680-8C>T	ENSP00000499852.1:n.680-8C>T
ENST00000345378.6:c.683-8C>T	ENSP00000223366.2:n.683-8C>T
ENST00000395796.7:c.677-8C>T	ENSP00000379142.3:n.677-8C>T
ENST00000403799.7:c.680-8C>T	ENSP00000384247.3:n.680-8C>T
ENST00000437084.1:c.629-8C>T	ENSP00000402840.1:n.629-8C>T
ENST00000616242.4:c.677-8C>T	ENSP00000482149.1:n.677-8C>T
NM_000162.3:c.680-8C>T	NP_000153.1:n.680-8C>T
NM_033507.1:c.683-8C>T	NP_277042.1:n.683-8C>T
NM_033508.1:c.677-8C>T	NP_277043.1:n.677-8C>T
XR_927223.1:n.82+93G>A
NM_000162.4:c.680-8C>T	NP_000153.1:n.680-8C>T
NM_001354800.1:c.680-8C>T	NP_001341729.1:n.680-8C>T
NM_033507.2:c.683-8C>T	NP_277042.1:n.683-8C>T
NM_033508.2:c.677-8C>T	NP_277043.1:n.677-8C>T
XR_927223.2:n.82+93G>A
NM_000162.5:c.680-8C>T MANE Select	NP_000153.1:n.680-8C>T
NM_033507.3:c.683-8C>T	NP_277042.1:n.683-8C>T
NM_033508.3:c.677-8C>T	NP_277043.1:n.677-8C>T