Canonical Allele Identifier: CA367402032

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44190617G>A (hg19) ; chr7:g.44151018G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44151018G>A , CM000669.2:g.44151018G>A	GRCh38
NC_000007.13:g.44190617G>A , CM000669.1:g.44190617G>A	GRCh37
NC_000007.12:g.44157142G>A	NCBI36
NG_008847.1:g.43406C>T
NG_008847.2:g.52153C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*419C>T	ENSP00000379142.4:n.*419C>T
ENST00000616242.5:c.421C>T	ENSP00000482149.2:p.His141Tyr
ENST00000682635.1:n.907C>T
ENST00000345378.7:c.424C>T	ENSP00000223366.2:p.His142Tyr
ENST00000403799.8:c.421C>T MANE Select	ENSP00000384247.3:p.His141Tyr
ENST00000671824.1:c.421C>T	ENSP00000500264.1:p.His141Tyr
ENST00000673284.1:c.421C>T	ENSP00000499852.1:p.His141Tyr
ENST00000345378.6:c.424C>T	ENSP00000223366.2:p.His142Tyr
ENST00000395796.7:c.418C>T	ENSP00000379142.3:p.His140Tyr
ENST00000403799.7:c.421C>T	ENSP00000384247.3:p.His141Tyr
ENST00000437084.1:c.370C>T	ENSP00000402840.1:p.His124Tyr
ENST00000616242.4:c.418C>T	ENSP00000482149.1:p.His140Tyr
NM_000162.3:c.421C>T	NP_000153.1:p.His141Tyr
NM_033507.1:c.424C>T	NP_277042.1:p.His142Tyr
NM_033508.1:c.418C>T	NP_277043.1:p.His140Tyr
NM_000162.4:c.421C>T	NP_000153.1:p.His141Tyr
NM_001354800.1:c.421C>T	NP_001341729.1:p.His141Tyr
NM_033507.2:c.424C>T	NP_277042.1:p.His142Tyr
NM_033508.2:c.418C>T	NP_277043.1:p.His140Tyr
NM_000162.5:c.421C>T MANE Select	NP_000153.1:p.His141Tyr
NM_033507.3:c.424C>T	NP_277042.1:p.His142Tyr
NM_033508.3:c.418C>T	NP_277043.1:p.His140Tyr