Canonical Allele Identifier: CA157919467

Gene: GCK

Linked Data

• dbSNP Id: rs148157961
• gnomAD v2: 7-44192176-C-G
• gnomAD v3: 7-44152577-C-G
• gnomAD v4: 7-44152577-C-G
• MyVariant Identifiers: chr7:g.44192176C>G (hg19) ; chr7:g.44152577C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152577C>G , CM000669.2:g.44152577C>G	GRCh38
NC_000007.13:g.44192176C>G , CM000669.1:g.44192176C>G	GRCh37
NC_000007.12:g.44158701C>G	NCBI36
NG_008847.1:g.41847G>C
NG_008847.2:g.50594G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*207-152G>C	ENSP00000379142.4:n.*207-152G>C
ENST00000616242.5:c.209-152G>C	ENSP00000482149.2:n.209-152G>C
ENST00000682635.1:n.695-152G>C
ENST00000345378.7:c.212-152G>C	ENSP00000223366.2:n.212-152G>C
ENST00000403799.8:c.209-152G>C MANE Select	ENSP00000384247.3:n.209-152G>C
ENST00000671824.1:c.209-152G>C	ENSP00000500264.1:n.209-152G>C
ENST00000673284.1:c.209-152G>C	ENSP00000499852.1:n.209-152G>C
ENST00000345378.6:c.212-152G>C	ENSP00000223366.2:n.212-152G>C
ENST00000395796.7:c.206-152G>C	ENSP00000379142.3:n.206-152G>C
ENST00000403799.7:c.209-152G>C	ENSP00000384247.3:n.209-152G>C
ENST00000437084.1:c.209-152G>C	ENSP00000402840.1:n.209-152G>C
ENST00000616242.4:c.206-152G>C	ENSP00000482149.1:n.206-152G>C
NM_000162.3:c.209-152G>C	NP_000153.1:n.209-152G>C
NM_033507.1:c.212-152G>C	NP_277042.1:n.212-152G>C
NM_033508.1:c.206-152G>C	NP_277043.1:n.206-152G>C
NM_000162.4:c.209-152G>C	NP_000153.1:n.209-152G>C
NM_001354800.1:c.209-152G>C	NP_001341729.1:n.209-152G>C
NM_033507.2:c.212-152G>C	NP_277042.1:n.212-152G>C
NM_033508.2:c.206-152G>C	NP_277043.1:n.206-152G>C
NM_000162.5:c.209-152G>C MANE Select	NP_000153.1:n.209-152G>C
NM_033507.3:c.212-152G>C	NP_277042.1:n.212-152G>C
NM_033508.3:c.206-152G>C	NP_277043.1:n.206-152G>C