Canonical Allele Identifier: CA454609152

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44189438C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149839C>A , CM000669.2:g.44149839C>A	GRCh38
NC_000007.13:g.44189438C>A , CM000669.1:g.44189438C>A	GRCh37
NC_000007.12:g.44155963C>A	NCBI36
NG_008847.1:g.44585G>T
NG_008847.2:g.53332G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*598G>T	ENSP00000379142.4:n.*598G>T
ENST00000616242.5:c.600G>T	ENSP00000482149.2:p.Val200=
ENST00000682635.1:n.1086G>T
ENST00000345378.7:c.603G>T	ENSP00000223366.2:p.Val201=
ENST00000403799.8:c.600G>T MANE Select	ENSP00000384247.3:p.Val200=
ENST00000671824.1:c.600G>T	ENSP00000500264.1:p.Val200=
ENST00000673284.1:c.600G>T	ENSP00000499852.1:p.Val200=
ENST00000345378.6:c.603G>T	ENSP00000223366.2:p.Val201=
ENST00000395796.7:c.597G>T	ENSP00000379142.3:p.Val199=
ENST00000403799.7:c.600G>T	ENSP00000384247.3:p.Val200=
ENST00000437084.1:c.549G>T	ENSP00000402840.1:p.Val183=
ENST00000616242.4:c.597G>T	ENSP00000482149.1:p.Val199=
NM_000162.3:c.600G>T	NP_000153.1:p.Val200=
NM_033507.1:c.603G>T	NP_277042.1:p.Val201=
NM_033508.1:c.597G>T	NP_277043.1:p.Val199=
NM_000162.4:c.600G>T	NP_000153.1:p.Val200=
NM_001354800.1:c.600G>T	NP_001341729.1:p.Val200=
NM_033507.2:c.603G>T	NP_277042.1:p.Val201=
NM_033508.2:c.597G>T	NP_277043.1:p.Val199=
NM_000162.5:c.600G>T MANE Select	NP_000153.1:p.Val200=
NM_033507.3:c.603G>T	NP_277042.1:p.Val201=
NM_033508.3:c.597G>T	NP_277043.1:p.Val199=