Canonical Allele Identifier: CA341344070

Gene: AGL

Linked Data

• MyVariant Identifiers: chr1:g.100387201T>A (hg19) ; chr1:g.99921645T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921645T>A , CM000663.2:g.99921645T>A	GRCh38
NC_000001.10:g.100387201T>A , CM000663.1:g.100387201T>A	GRCh37
NC_000001.9:g.100159789T>A	NCBI36
NG_012865.1:g.76562T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4593T>A MANE Select	ENSP00000355106.3:p.Asp1531Glu
ENST00000637337.1:n.4804T>A
ENST00000294724.8:c.4593T>A	ENSP00000294724.4:p.Asp1531Glu
ENST00000361302.7:c.4545T>A	ENSP00000354971.3:p.Asp1515Glu
ENST00000361522.4:c.4542T>A	ENSP00000354635.4:p.Asp1514Glu
ENST00000361915.7:c.4593T>A	ENSP00000355106.3:p.Asp1531Glu
ENST00000370161.6:c.4545T>A	ENSP00000359180.2:p.Asp1515Glu
ENST00000370163.7:c.4593T>A	ENSP00000359182.3:p.Asp1531Glu
ENST00000370165.7:c.4593T>A	ENSP00000359184.3:p.Asp1531Glu
NM_000028.2:c.4593T>A	NP_000019.2:p.Asp1531Glu
NM_000642.2:c.4593T>A	NP_000633.2:p.Asp1531Glu
NM_000643.2:c.4593T>A	NP_000634.2:p.Asp1531Glu
NM_000644.2:c.4593T>A	NP_000635.2:p.Asp1531Glu
NM_000645.2:c.4542T>A	NP_000636.2:p.Asp1514Glu
NM_000646.2:c.4545T>A	NP_000637.2:p.Asp1515Glu
XM_005270557.1:c.4593T>A	XP_005270614.1:p.Asp1531Glu
XR_947626.1:n.1317+2593A>T
XR_947627.1:n.1206+2593A>T
XR_947628.1:n.1311+2593A>T
XR_947630.1:n.1249+2593A>T
XR_947632.1:n.1135+2593A>T
XR_947633.1:n.1246+2593A>T
XR_947634.1:n.660+2593A>T
XR_947635.1:n.728+2593A>T
XM_005270557.2:c.4593T>A	XP_005270614.1:p.Asp1531Glu
XM_017000501.2:c.2853T>A	XP_016855990.1:p.Asp951Glu
NM_000642.3:c.4593T>A MANE Select	NP_000633.2:p.Asp1531Glu