Canonical Allele Identifier: CA1703637000

Gene: GCK

Linked Data

• dbSNP Id: rs2096281470
• gnomAD v4: 7-44152232-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152232A>G , CM000669.2:g.44152232A>G	GRCh38
NC_000007.13:g.44191831A>G , CM000669.1:g.44191831A>G	GRCh37
NC_000007.12:g.44158356A>G	NCBI36
NG_008847.1:g.42192T>C
NG_008847.2:g.50939T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*361+39T>C	ENSP00000379142.4:n.*361+39T>C
ENST00000616242.5:c.363+39T>C	ENSP00000482149.2:n.363+39T>C
ENST00000682635.1:n.849+39T>C
ENST00000345378.7:c.366+39T>C	ENSP00000223366.2:n.366+39T>C
ENST00000403799.8:c.363+39T>C MANE Select	ENSP00000384247.3:n.363+39T>C
ENST00000671824.1:c.363+39T>C	ENSP00000500264.1:n.363+39T>C
ENST00000673284.1:c.363+39T>C	ENSP00000499852.1:n.363+39T>C
ENST00000345378.6:c.366+39T>C	ENSP00000223366.2:n.366+39T>C
ENST00000395796.7:c.360+39T>C	ENSP00000379142.3:n.360+39T>C
ENST00000403799.7:c.363+39T>C	ENSP00000384247.3:n.363+39T>C
ENST00000437084.1:c.363+39T>C	ENSP00000402840.1:n.363+39T>C
ENST00000616242.4:c.360+39T>C	ENSP00000482149.1:n.360+39T>C
NM_000162.3:c.363+39T>C	NP_000153.1:n.363+39T>C
NM_033507.1:c.366+39T>C	NP_277042.1:n.366+39T>C
NM_033508.1:c.360+39T>C	NP_277043.1:n.360+39T>C
NM_000162.4:c.363+39T>C	NP_000153.1:n.363+39T>C
NM_001354800.1:c.363+39T>C	NP_001341729.1:n.363+39T>C
NM_033507.2:c.366+39T>C	NP_277042.1:n.366+39T>C
NM_033508.2:c.360+39T>C	NP_277043.1:n.360+39T>C
NM_000162.5:c.363+39T>C MANE Select	NP_000153.1:n.363+39T>C
NM_033507.3:c.366+39T>C	NP_277042.1:n.366+39T>C
NM_033508.3:c.360+39T>C	NP_277043.1:n.360+39T>C