Canonical Allele Identifier: CA454607746

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44186082G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146483G>A , CM000669.2:g.44146483G>A	GRCh38
NC_000007.13:g.44186082G>A , CM000669.1:g.44186082G>A	GRCh37
NC_000007.12:g.44152607G>A	NCBI36
NG_008847.1:g.47941C>T
NG_008847.2:g.56688C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*997C>T	ENSP00000379142.4:n.*997C>T
ENST00000616242.5:c.*119C>T	ENSP00000482149.2:n.*119C>T
ENST00000683378.1:n.225C>T
ENST00000345378.7:c.1002C>T	ENSP00000223366.2:p.Arg334=
ENST00000403799.8:c.999C>T MANE Select	ENSP00000384247.3:p.Arg333=
ENST00000671824.1:c.1062C>T	ENSP00000500264.1:p.Arg354=
ENST00000673284.1:c.999C>T	ENSP00000499852.1:p.Arg333=
ENST00000345378.6:c.1002C>T	ENSP00000223366.2:p.Arg334=
ENST00000395796.7:c.996C>T	ENSP00000379142.3:p.Arg332=
ENST00000403799.7:c.999C>T	ENSP00000384247.3:p.Arg333=
ENST00000437084.1:c.948C>T	ENSP00000402840.1:p.Arg316=
ENST00000473353.1:n.297C>T
ENST00000616242.4:c.996C>T	ENSP00000482149.1:p.Arg332=
NM_000162.3:c.999C>T	NP_000153.1:p.Arg333=
NM_033507.1:c.1002C>T	NP_277042.1:p.Arg334=
NM_033508.1:c.996C>T	NP_277043.1:p.Arg332=
NM_000162.4:c.999C>T	NP_000153.1:p.Arg333=
NM_001354800.1:c.999C>T	NP_001341729.1:p.Arg333=
NM_001354801.1:c.8+136C>T	NP_001341730.1:n.8+136C>T
NM_033507.2:c.1002C>T	NP_277042.1:p.Arg334=
NM_033508.2:c.996C>T	NP_277043.1:p.Arg332=
NM_000162.5:c.999C>T MANE Select	NP_000153.1:p.Arg333=
NM_033507.3:c.1002C>T	NP_277042.1:p.Arg334=
NM_033508.3:c.996C>T	NP_277043.1:p.Arg332=