Canonical Allele Identifier: CA367403270

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44192920C>G (hg19) ; chr7:g.44153321C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153321C>G , CM000669.2:g.44153321C>G	GRCh38
NC_000007.13:g.44192920C>G , CM000669.1:g.44192920C>G	GRCh37
NC_000007.12:g.44159445C>G	NCBI36
NG_008847.1:g.41103G>C
NG_008847.2:g.49850G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*186G>C	ENSP00000379142.4:n.*186G>C
ENST00000616242.5:c.188G>C	ENSP00000482149.2:p.Arg63Pro
ENST00000682635.1:n.674G>C
ENST00000345378.7:c.191G>C	ENSP00000223366.2:p.Arg64Pro
ENST00000403799.8:c.188G>C MANE Select	ENSP00000384247.3:p.Arg63Pro
ENST00000671824.1:c.188G>C	ENSP00000500264.1:p.Arg63Pro
ENST00000673284.1:c.188G>C	ENSP00000499852.1:p.Arg63Pro
ENST00000345378.6:c.191G>C	ENSP00000223366.2:p.Arg64Pro
ENST00000395796.7:c.185G>C	ENSP00000379142.3:p.Arg62Pro
ENST00000403799.7:c.188G>C	ENSP00000384247.3:p.Arg63Pro
ENST00000437084.1:c.188G>C	ENSP00000402840.1:p.Arg63Pro
ENST00000616242.4:c.185G>C	ENSP00000482149.1:p.Arg62Pro
NM_000162.3:c.188G>C	NP_000153.1:p.Arg63Pro
NM_033507.1:c.191G>C	NP_277042.1:p.Arg64Pro
NM_033508.1:c.185G>C	NP_277043.1:p.Arg62Pro
NM_000162.4:c.188G>C	NP_000153.1:p.Arg63Pro
NM_001354800.1:c.188G>C	NP_001341729.1:p.Arg63Pro
NM_033507.2:c.191G>C	NP_277042.1:p.Arg64Pro
NM_033508.2:c.185G>C	NP_277043.1:p.Arg62Pro
NM_000162.5:c.188G>C MANE Select	NP_000153.1:p.Arg63Pro
NM_033507.3:c.191G>C	NP_277042.1:p.Arg64Pro
NM_033508.3:c.185G>C	NP_277043.1:p.Arg62Pro