Canonical Allele Identifier: CA367403430

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44192972T>A (hg19) ; chr7:g.44153373T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153373T>A , CM000669.2:g.44153373T>A	GRCh38
NC_000007.13:g.44192972T>A , CM000669.1:g.44192972T>A	GRCh37
NC_000007.12:g.44159497T>A	NCBI36
NG_008847.1:g.41051A>T
NG_008847.2:g.49798A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*134A>T	ENSP00000379142.4:n.*134A>T
ENST00000616242.5:c.136A>T	ENSP00000482149.2:p.Arg46Trp
ENST00000682635.1:n.622A>T
ENST00000345378.7:c.139A>T	ENSP00000223366.2:p.Arg47Trp
ENST00000403799.8:c.136A>T MANE Select	ENSP00000384247.3:p.Arg46Trp
ENST00000671824.1:c.136A>T	ENSP00000500264.1:p.Arg46Trp
ENST00000673284.1:c.136A>T	ENSP00000499852.1:p.Arg46Trp
ENST00000345378.6:c.139A>T	ENSP00000223366.2:p.Arg47Trp
ENST00000395796.7:c.133A>T	ENSP00000379142.3:p.Arg45Trp
ENST00000403799.7:c.136A>T	ENSP00000384247.3:p.Arg46Trp
ENST00000437084.1:c.136A>T	ENSP00000402840.1:p.Arg46Trp
ENST00000616242.4:c.133A>T	ENSP00000482149.1:p.Arg45Trp
NM_000162.3:c.136A>T	NP_000153.1:p.Arg46Trp
NM_033507.1:c.139A>T	NP_277042.1:p.Arg47Trp
NM_033508.1:c.133A>T	NP_277043.1:p.Arg45Trp
NM_000162.4:c.136A>T	NP_000153.1:p.Arg46Trp
NM_001354800.1:c.136A>T	NP_001341729.1:p.Arg46Trp
NM_033507.2:c.139A>T	NP_277042.1:p.Arg47Trp
NM_033508.2:c.133A>T	NP_277043.1:p.Arg45Trp
NM_000162.5:c.136A>T MANE Select	NP_000153.1:p.Arg46Trp
NM_033507.3:c.139A>T	NP_277042.1:p.Arg47Trp
NM_033508.3:c.133A>T	NP_277043.1:p.Arg45Trp