Canonical Allele Identifier: CA341343624

Gene: AGL

Linked Data

• MyVariant Identifiers: chr1:g.100387142C>A (hg19) ; chr1:g.99921586C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921586C>A , CM000663.2:g.99921586C>A	GRCh38
NC_000001.10:g.100387142C>A , CM000663.1:g.100387142C>A	GRCh37
NC_000001.9:g.100159730C>A	NCBI36
NG_012865.1:g.76503C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4534C>A MANE Select	ENSP00000355106.3:p.Pro1512Thr
ENST00000637337.1:n.4745C>A
ENST00000294724.8:c.4534C>A	ENSP00000294724.4:p.Pro1512Thr
ENST00000361302.7:c.4486C>A	ENSP00000354971.3:p.Pro1496Thr
ENST00000361522.4:c.4483C>A	ENSP00000354635.4:p.Pro1495Thr
ENST00000361915.7:c.4534C>A	ENSP00000355106.3:p.Pro1512Thr
ENST00000370161.6:c.4486C>A	ENSP00000359180.2:p.Pro1496Thr
ENST00000370163.7:c.4534C>A	ENSP00000359182.3:p.Pro1512Thr
ENST00000370165.7:c.4534C>A	ENSP00000359184.3:p.Pro1512Thr
NM_000028.2:c.4534C>A	NP_000019.2:p.Pro1512Thr
NM_000642.2:c.4534C>A	NP_000633.2:p.Pro1512Thr
NM_000643.2:c.4534C>A	NP_000634.2:p.Pro1512Thr
NM_000644.2:c.4534C>A	NP_000635.2:p.Pro1512Thr
NM_000645.2:c.4483C>A	NP_000636.2:p.Pro1495Thr
NM_000646.2:c.4486C>A	NP_000637.2:p.Pro1496Thr
XM_005270557.1:c.4534C>A	XP_005270614.1:p.Pro1512Thr
XR_947626.1:n.1317+2652G>T
XR_947627.1:n.1206+2652G>T
XR_947628.1:n.1311+2652G>T
XR_947630.1:n.1249+2652G>T
XR_947632.1:n.1135+2652G>T
XR_947633.1:n.1246+2652G>T
XR_947634.1:n.660+2652G>T
XR_947635.1:n.728+2652G>T
XM_005270557.2:c.4534C>A	XP_005270614.1:p.Pro1512Thr
XM_017000501.2:c.2794C>A	XP_016855990.1:p.Pro932Thr
NM_000642.3:c.4534C>A MANE Select	NP_000633.2:p.Pro1512Thr