Canonical Allele Identifier: CA157917140

Gene: GCK

Linked Data

• dbSNP Id: rs919583645
• gnomAD v3: 7-44149654-A-G
• gnomAD v4: 7-44149654-A-G
• MyVariant Identifiers: chr7:g.44189253A>G (hg19) ; chr7:g.44149654A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149654A>G , CM000669.2:g.44149654A>G	GRCh38
NC_000007.13:g.44189253A>G , CM000669.1:g.44189253A>G	GRCh37
NC_000007.12:g.44155778A>G	NCBI36
NG_008847.1:g.44770T>C
NG_008847.2:g.53517T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*677+106T>C	ENSP00000379142.4:n.*677+106T>C
ENST00000616242.5:c.679+106T>C	ENSP00000482149.2:n.679+106T>C
ENST00000682635.1:n.1271T>C
ENST00000345378.7:c.682+106T>C	ENSP00000223366.2:n.682+106T>C
ENST00000403799.8:c.679+106T>C MANE Select	ENSP00000384247.3:n.679+106T>C
ENST00000671824.1:c.679+106T>C	ENSP00000500264.1:n.679+106T>C
ENST00000673284.1:c.679+106T>C	ENSP00000499852.1:n.679+106T>C
ENST00000345378.6:c.682+106T>C	ENSP00000223366.2:n.682+106T>C
ENST00000395796.7:c.676+106T>C	ENSP00000379142.3:n.676+106T>C
ENST00000403799.7:c.679+106T>C	ENSP00000384247.3:n.679+106T>C
ENST00000437084.1:c.628+106T>C	ENSP00000402840.1:n.628+106T>C
ENST00000616242.4:c.676+106T>C	ENSP00000482149.1:n.676+106T>C
NM_000162.3:c.679+106T>C	NP_000153.1:n.679+106T>C
NM_033507.1:c.682+106T>C	NP_277042.1:n.682+106T>C
NM_033508.1:c.676+106T>C	NP_277043.1:n.676+106T>C
XR_927223.1:n.204-35A>G
NM_000162.4:c.679+106T>C	NP_000153.1:n.679+106T>C
NM_001354800.1:c.679+106T>C	NP_001341729.1:n.679+106T>C
NM_033507.2:c.682+106T>C	NP_277042.1:n.682+106T>C
NM_033508.2:c.676+106T>C	NP_277043.1:n.676+106T>C
XR_927223.2:n.204-35A>G
NM_000162.5:c.679+106T>C MANE Select	NP_000153.1:n.679+106T>C
NM_033507.3:c.682+106T>C	NP_277042.1:n.682+106T>C
NM_033508.3:c.676+106T>C	NP_277043.1:n.676+106T>C