Canonical Allele Identifier: CA367403264

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44192918A>T (hg19) ; chr7:g.44153319A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153319A>T , CM000669.2:g.44153319A>T	GRCh38
NC_000007.13:g.44192918A>T , CM000669.1:g.44192918A>T	GRCh37
NC_000007.12:g.44159443A>T	NCBI36
NG_008847.1:g.41105T>A
NG_008847.2:g.49852T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*188T>A	ENSP00000379142.4:n.*188T>A
ENST00000616242.5:c.190T>A	ENSP00000482149.2:p.Ser64Thr
ENST00000682635.1:n.676T>A
ENST00000345378.7:c.193T>A	ENSP00000223366.2:p.Ser65Thr
ENST00000403799.8:c.190T>A MANE Select	ENSP00000384247.3:p.Ser64Thr
ENST00000671824.1:c.190T>A	ENSP00000500264.1:p.Ser64Thr
ENST00000673284.1:c.190T>A	ENSP00000499852.1:p.Ser64Thr
ENST00000345378.6:c.193T>A	ENSP00000223366.2:p.Ser65Thr
ENST00000395796.7:c.187T>A	ENSP00000379142.3:p.Ser63Thr
ENST00000403799.7:c.190T>A	ENSP00000384247.3:p.Ser64Thr
ENST00000437084.1:c.190T>A	ENSP00000402840.1:p.Ser64Thr
ENST00000616242.4:c.187T>A	ENSP00000482149.1:p.Ser63Thr
NM_000162.3:c.190T>A	NP_000153.1:p.Ser64Thr
NM_033507.1:c.193T>A	NP_277042.1:p.Ser65Thr
NM_033508.1:c.187T>A	NP_277043.1:p.Ser63Thr
NM_000162.4:c.190T>A	NP_000153.1:p.Ser64Thr
NM_001354800.1:c.190T>A	NP_001341729.1:p.Ser64Thr
NM_033507.2:c.193T>A	NP_277042.1:p.Ser65Thr
NM_033508.2:c.187T>A	NP_277043.1:p.Ser63Thr
NM_000162.5:c.190T>A MANE Select	NP_000153.1:p.Ser64Thr
NM_033507.3:c.193T>A	NP_277042.1:p.Ser65Thr
NM_033508.3:c.187T>A	NP_277043.1:p.Ser63Thr