Canonical Allele Identifier: CA2682588732

Gene: GCK

Linked Data

• gnomAD v4: 7-44147626-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147626T>C , CM000669.2:g.44147626T>C	GRCh38
NC_000007.13:g.44187225T>C , CM000669.1:g.44187225T>C	GRCh37
NC_000007.12:g.44153750T>C	NCBI36
NG_008847.1:g.46798A>G
NG_008847.2:g.55545A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*861+24A>G	ENSP00000379142.4:n.*861+24A>G
ENST00000616242.5:c.853+34A>G	ENSP00000482149.2:n.853+34A>G
ENST00000345378.7:c.866+24A>G	ENSP00000223366.2:n.866+24A>G
ENST00000403799.8:c.863+24A>G MANE Select	ENSP00000384247.3:n.863+24A>G
ENST00000671824.1:c.853+34A>G	ENSP00000500264.1:n.853+34A>G
ENST00000673284.1:c.863+24A>G	ENSP00000499852.1:n.863+24A>G
ENST00000345378.6:c.866+24A>G	ENSP00000223366.2:n.866+24A>G
ENST00000395796.7:c.860+24A>G	ENSP00000379142.3:n.860+24A>G
ENST00000403799.7:c.863+24A>G	ENSP00000384247.3:n.863+24A>G
ENST00000437084.1:c.812+24A>G	ENSP00000402840.1:n.812+24A>G
ENST00000616242.4:c.860+24A>G	ENSP00000482149.1:n.860+24A>G
NM_000162.3:c.863+24A>G	NP_000153.1:n.863+24A>G
NM_033507.1:c.866+24A>G	NP_277042.1:n.866+24A>G
NM_033508.1:c.860+24A>G	NP_277043.1:n.860+24A>G
NM_000162.4:c.863+24A>G	NP_000153.1:n.863+24A>G
NM_001354800.1:c.863+24A>G	NP_001341729.1:n.863+24A>G
NM_033507.2:c.866+24A>G	NP_277042.1:n.866+24A>G
NM_033508.2:c.860+24A>G	NP_277043.1:n.860+24A>G
NM_000162.5:c.863+24A>G MANE Select	NP_000153.1:n.863+24A>G
NM_033507.3:c.866+24A>G	NP_277042.1:n.866+24A>G
NM_033508.3:c.860+24A>G	NP_277043.1:n.860+24A>G