Canonical Allele Identifier: CA4239505

Gene: GCK

Linked Data

• dbSNP Id: rs777953506
• ExAC: 7:44187223 G / C
• gnomAD v2: 7-44187223-G-C
• gnomAD v3: 7-44147624-G-C
• gnomAD v4: 7-44147624-G-C
• MyVariant Identifiers: chr7:g.44187223G>C (hg19) ; chr7:g.44147624G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147624G>C , CM000669.2:g.44147624G>C	GRCh38
NC_000007.13:g.44187223G>C , CM000669.1:g.44187223G>C	GRCh37
NC_000007.12:g.44153748G>C	NCBI36
NG_008847.1:g.46800C>G
NG_008847.2:g.55547C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*861+26C>G	ENSP00000379142.4:n.*861+26C>G
ENST00000616242.5:c.853+36C>G	ENSP00000482149.2:n.853+36C>G
ENST00000345378.7:c.866+26C>G	ENSP00000223366.2:n.866+26C>G
ENST00000403799.8:c.863+26C>G MANE Select	ENSP00000384247.3:n.863+26C>G
ENST00000671824.1:c.853+36C>G	ENSP00000500264.1:n.853+36C>G
ENST00000673284.1:c.863+26C>G	ENSP00000499852.1:n.863+26C>G
ENST00000345378.6:c.866+26C>G	ENSP00000223366.2:n.866+26C>G
ENST00000395796.7:c.860+26C>G	ENSP00000379142.3:n.860+26C>G
ENST00000403799.7:c.863+26C>G	ENSP00000384247.3:n.863+26C>G
ENST00000437084.1:c.812+26C>G	ENSP00000402840.1:n.812+26C>G
ENST00000616242.4:c.860+26C>G	ENSP00000482149.1:n.860+26C>G
NM_000162.3:c.863+26C>G	NP_000153.1:n.863+26C>G
NM_033507.1:c.866+26C>G	NP_277042.1:n.866+26C>G
NM_033508.1:c.860+26C>G	NP_277043.1:n.860+26C>G
NM_000162.4:c.863+26C>G	NP_000153.1:n.863+26C>G
NM_001354800.1:c.863+26C>G	NP_001341729.1:n.863+26C>G
NM_033507.2:c.866+26C>G	NP_277042.1:n.866+26C>G
NM_033508.2:c.860+26C>G	NP_277043.1:n.860+26C>G
NM_000162.5:c.863+26C>G MANE Select	NP_000153.1:n.863+26C>G
NM_033507.3:c.866+26C>G	NP_277042.1:n.866+26C>G
NM_033508.3:c.860+26C>G	NP_277043.1:n.860+26C>G