Canonical Allele Identifier: CA367401225

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44189388T>A (hg19) ; chr7:g.44149789T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149789T>A , CM000669.2:g.44149789T>A	GRCh38
NC_000007.13:g.44189388T>A , CM000669.1:g.44189388T>A	GRCh37
NC_000007.12:g.44155913T>A	NCBI36
NG_008847.1:g.44635A>T
NG_008847.2:g.53382A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*648A>T	ENSP00000379142.4:n.*648A>T
ENST00000616242.5:c.650A>T	ENSP00000482149.2:p.Asp217Val
ENST00000682635.1:n.1136A>T
ENST00000345378.7:c.653A>T	ENSP00000223366.2:p.Asp218Val
ENST00000403799.8:c.650A>T MANE Select	ENSP00000384247.3:p.Asp217Val
ENST00000671824.1:c.650A>T	ENSP00000500264.1:p.Asp217Val
ENST00000673284.1:c.650A>T	ENSP00000499852.1:p.Asp217Val
ENST00000345378.6:c.653A>T	ENSP00000223366.2:p.Asp218Val
ENST00000395796.7:c.647A>T	ENSP00000379142.3:p.Asp216Val
ENST00000403799.7:c.650A>T	ENSP00000384247.3:p.Asp217Val
ENST00000437084.1:c.599A>T	ENSP00000402840.1:p.Asp200Val
ENST00000616242.4:c.647A>T	ENSP00000482149.1:p.Asp216Val
NM_000162.3:c.650A>T	NP_000153.1:p.Asp217Val
NM_033507.1:c.653A>T	NP_277042.1:p.Asp218Val
NM_033508.1:c.647A>T	NP_277043.1:p.Asp216Val
NM_000162.4:c.650A>T	NP_000153.1:p.Asp217Val
NM_001354800.1:c.650A>T	NP_001341729.1:p.Asp217Val
NM_033507.2:c.653A>T	NP_277042.1:p.Asp218Val
NM_033508.2:c.647A>T	NP_277043.1:p.Asp216Val
NM_000162.5:c.650A>T MANE Select	NP_000153.1:p.Asp217Val
NM_033507.3:c.653A>T	NP_277042.1:p.Asp218Val
NM_033508.3:c.647A>T	NP_277043.1:p.Asp216Val