Canonical Allele Identifier: CA454610232

Gene: GCK

Linked Data

• gnomAD v4: 7-44152331-C-T
• COSMIC: COSM6177797 ; COSM6177798 ; COSM6177799
• MyVariant Identifiers: chr7:g.44191930C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152331C>T , CM000669.2:g.44152331C>T	GRCh38
NC_000007.13:g.44191930C>T , CM000669.1:g.44191930C>T	GRCh37
NC_000007.12:g.44158455C>T	NCBI36
NG_008847.1:g.42093G>A
NG_008847.2:g.50840G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*301G>A	ENSP00000379142.4:n.*301G>A
ENST00000616242.5:c.303G>A	ENSP00000482149.2:p.Val101=
ENST00000682635.1:n.789G>A
ENST00000345378.7:c.306G>A	ENSP00000223366.2:p.Val102=
ENST00000403799.8:c.303G>A MANE Select	ENSP00000384247.3:p.Val101=
ENST00000671824.1:c.303G>A	ENSP00000500264.1:p.Val101=
ENST00000673284.1:c.303G>A	ENSP00000499852.1:p.Val101=
ENST00000345378.6:c.306G>A	ENSP00000223366.2:p.Val102=
ENST00000395796.7:c.300G>A	ENSP00000379142.3:p.Val100=
ENST00000403799.7:c.303G>A	ENSP00000384247.3:p.Val101=
ENST00000437084.1:c.303G>A	ENSP00000402840.1:p.Val101=
ENST00000616242.4:c.300G>A	ENSP00000482149.1:p.Val100=
NM_000162.3:c.303G>A	NP_000153.1:p.Val101=
NM_033507.1:c.306G>A	NP_277042.1:p.Val102=
NM_033508.1:c.300G>A	NP_277043.1:p.Val100=
NM_000162.4:c.303G>A	NP_000153.1:p.Val101=
NM_001354800.1:c.303G>A	NP_001341729.1:p.Val101=
NM_033507.2:c.306G>A	NP_277042.1:p.Val102=
NM_033508.2:c.300G>A	NP_277043.1:p.Val100=
NM_000162.5:c.303G>A MANE Select	NP_000153.1:p.Val101=
NM_033507.3:c.306G>A	NP_277042.1:p.Val102=
NM_033508.3:c.300G>A	NP_277043.1:p.Val100=