Canonical Allele Identifier: CA1183926855

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99875412C= , CM000663.2:g.99875412C=	GRCh38
NC_000001.10:g.100340968C= , CM000663.1:g.100340968C=	GRCh37
NC_000001.9:g.100113556C=	NCBI36
NG_012865.1:g.30329C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1240C= MANE Select	ENSP00000355106.3:p.Pro414=
ENST00000637337.1:n.1451C=
ENST00000294724.8:c.1240C=	ENSP00000294724.4:p.Pro414=
ENST00000361302.7:c.1192C=	ENSP00000354971.3:p.Pro398=
ENST00000361522.4:c.1189C=	ENSP00000354635.4:p.Pro397=
ENST00000361915.7:c.1240C=	ENSP00000355106.3:p.Pro414=
ENST00000370161.6:c.1192C=	ENSP00000359180.2:p.Pro398=
ENST00000370163.7:c.1240C=	ENSP00000359182.3:p.Pro414=
ENST00000370165.7:c.1240C=	ENSP00000359184.3:p.Pro414=
ENST00000477753.1:n.499C=
NM_000028.2:c.1240C=	NP_000019.2:p.Pro414=
NM_000642.2:c.1240C=	NP_000633.2:p.Pro414=
NM_000643.2:c.1240C=	NP_000634.2:p.Pro414=
NM_000644.2:c.1240C=	NP_000635.2:p.Pro414=
NM_000645.2:c.1189C=	NP_000636.2:p.Pro397=
NM_000646.2:c.1192C=	NP_000637.2:p.Pro398=
XM_005270557.1:c.1240C=	XP_005270614.1:p.Pro414=
XM_005270557.2:c.1240C=	XP_005270614.1:p.Pro414=
NM_000642.3:c.1240C= MANE Select	NP_000633.2:p.Pro414=