Canonical Allele Identifier: CA1183923228

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99870549C= , CM000663.2:g.99870549C=	GRCh38
NC_000001.10:g.100336105C= , CM000663.1:g.100336105C=	GRCh37
NC_000001.9:g.100108693C=	NCBI36
NG_012865.1:g.25466C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.814C= MANE Select	ENSP00000355106.3:p.Pro272=
ENST00000637337.1:n.1025C=
ENST00000294724.8:c.814C=	ENSP00000294724.4:p.Pro272=
ENST00000361302.7:c.766C=	ENSP00000354971.3:p.Pro256=
ENST00000361522.4:c.763C=	ENSP00000354635.4:p.Pro255=
ENST00000361915.7:c.814C=	ENSP00000355106.3:p.Pro272=
ENST00000370161.6:c.766C=	ENSP00000359180.2:p.Pro256=
ENST00000370163.7:c.814C=	ENSP00000359182.3:p.Pro272=
ENST00000370165.7:c.814C=	ENSP00000359184.3:p.Pro272=
NM_000028.2:c.814C=	NP_000019.2:p.Pro272=
NM_000642.2:c.814C=	NP_000633.2:p.Pro272=
NM_000643.2:c.814C=	NP_000634.2:p.Pro272=
NM_000644.2:c.814C=	NP_000635.2:p.Pro272=
NM_000645.2:c.763C=	NP_000636.2:p.Pro255=
NM_000646.2:c.766C=	NP_000637.2:p.Pro256=
XM_005270557.1:c.814C=	XP_005270614.1:p.Pro272=
XM_005270557.2:c.814C=	XP_005270614.1:p.Pro272=
NM_000642.3:c.814C= MANE Select	NP_000633.2:p.Pro272=