Canonical Allele Identifier: CA1183923191

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99870517T= , CM000663.2:g.99870517T=	GRCh38
NC_000001.10:g.100336073T= , CM000663.1:g.100336073T=	GRCh37
NC_000001.9:g.100108661T=	NCBI36
NG_012865.1:g.25434T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.782T= MANE Select	ENSP00000355106.3:p.Val261=
ENST00000637337.1:n.993T=
ENST00000294724.8:c.782T=	ENSP00000294724.4:p.Val261=
ENST00000361302.7:c.734T=	ENSP00000354971.3:p.Val245=
ENST00000361522.4:c.731T=	ENSP00000354635.4:p.Val244=
ENST00000361915.7:c.782T=	ENSP00000355106.3:p.Val261=
ENST00000370161.6:c.734T=	ENSP00000359180.2:p.Val245=
ENST00000370163.7:c.782T=	ENSP00000359182.3:p.Val261=
ENST00000370165.7:c.782T=	ENSP00000359184.3:p.Val261=
NM_000028.2:c.782T=	NP_000019.2:p.Val261=
NM_000642.2:c.782T=	NP_000633.2:p.Val261=
NM_000643.2:c.782T=	NP_000634.2:p.Val261=
NM_000644.2:c.782T=	NP_000635.2:p.Val261=
NM_000645.2:c.731T=	NP_000636.2:p.Val244=
NM_000646.2:c.734T=	NP_000637.2:p.Val245=
XM_005270557.1:c.782T=	XP_005270614.1:p.Val261=
XM_005270557.2:c.782T=	XP_005270614.1:p.Val261=
NM_000642.3:c.782T= MANE Select	NP_000633.2:p.Val261=