Canonical Allele Identifier: CA10337204

Gene: GYG2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.2861554G>A , CM000685.2:g.2861554G>A	GRCh38
NC_000023.10:g.2779595G>A , CM000685.1:g.2779595G>A	GRCh37
NC_000023.9:g.2789595G>A	NCBI36
NG_021257.1:g.37733G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398806.8:c.870G>A MANE Select	ENSP00000381786.3:p.Ala290=
ENST00000639373.1:c.963G>A	ENSP00000491962.1:p.Ala321=
ENST00000353656.10:c.963G>A	ENSP00000487294.1:p.Ala321=
ENST00000381157.2:c.418G>A
ENST00000381161.5:n.918G>A
ENST00000381163.7:c.963G>A	ENSP00000370555.3:p.Ala321=
ENST00000398806.7:c.870G>A	ENSP00000381786.3:p.Ala290=
ENST00000453106.1:n.641G>A
NM_001079855.1:c.870G>A	NP_001073324.1:p.Ala290=
NM_001184702.1:c.870G>A	NP_001171631.1:p.Ala290=
NM_001184703.1:c.963G>A	NP_001171632.1:p.Ala321=
NM_001184704.1:c.405G>A	NP_001171633.1:p.Ala135=
NM_003918.2:c.963G>A	NP_003909.2:p.Ala321=
XM_006724521.2:c.963G>A	XP_006724584.1:p.Ala321=
XM_011545600.1:c.870G>A	XP_011543902.1:p.Ala290=
XM_011545601.1:c.957G>A	XP_011543903.1:p.Ala319=
XM_011545602.1:c.405G>A	XP_011543904.1:p.Ala135=
XM_011545600.2:c.870G>A	XP_011543902.1:p.Ala290=
XM_017029927.1:c.963G>A	XP_016885416.1:p.Ala321=
XM_017029928.1:c.963G>A	XP_016885417.1:p.Ala321=
XM_017029929.1:c.963G>A	XP_016885418.1:p.Ala321=
XM_017029930.1:c.870G>A	XP_016885419.1:p.Ala290=
XM_017029931.1:c.870G>A	XP_016885420.1:p.Ala290=
NM_001079855.2:c.870G>A MANE Select	NP_001073324.1:p.Ala290=
NM_001184702.2:c.870G>A	NP_001171631.1:p.Ala290=
NM_001184703.2:c.963G>A	NP_001171632.1:p.Ala321=
NM_001184704.2:c.405G>A	NP_001171633.1:p.Ala135=
NM_003918.3:c.963G>A	NP_003909.2:p.Ala321=