Canonical Allele Identifier: CA1183917090

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99851042A= , CM000663.2:g.99851042A=	GRCh38
NC_000001.10:g.100316598A= , CM000663.1:g.100316598A=	GRCh37
NC_000001.9:g.100089186A=	NCBI36
NG_012865.1:g.5959A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.-1A= MANE Select	ENSP00000355106.3:n.-1A=
ENST00000294724.8:c.-1A=	ENSP00000294724.4:n.-1A=
ENST00000361302.7:c.-192A=	ENSP00000354971.3:n.-192A=
ENST00000361915.7:c.-1A=	ENSP00000355106.3:n.-1A=
ENST00000370163.7:c.-1A=	ENSP00000359182.3:n.-1A=
ENST00000370165.7:c.-1A=	ENSP00000359184.3:n.-1A=
NM_000028.2:c.-1A=	NP_000019.2:n.-1A=
NM_000642.2:c.-1A=	NP_000633.2:n.-1A=
NM_000643.2:c.-1A=	NP_000634.2:n.-1A=
NM_000644.2:c.-1A=	NP_000635.2:n.-1A=
NM_000646.2:c.-192A=	NP_000637.2:n.-192A=
XM_005270557.1:c.-1A=	XP_005270614.1:n.-1A=
XM_005270557.2:c.-1A=	XP_005270614.1:n.-1A=
NM_000642.3:c.-1A= MANE Select	NP_000633.2:n.-1A=