Canonical Allele Identifier: CA1183927353

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99876579C= , CM000663.2:g.99876579C=	GRCh38
NC_000001.10:g.100342135C= , CM000663.1:g.100342135C=	GRCh37
NC_000001.9:g.100114723C=	NCBI36
NG_012865.1:g.31496C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1405C= MANE Select	ENSP00000355106.3:p.Arg469=
ENST00000637337.1:n.1616C=
ENST00000294724.8:c.1405C=	ENSP00000294724.4:p.Arg469=
ENST00000361302.7:c.1357C=	ENSP00000354971.3:p.Arg453=
ENST00000361522.4:c.1354C=	ENSP00000354635.4:p.Arg452=
ENST00000361915.7:c.1405C=	ENSP00000355106.3:p.Arg469=
ENST00000370161.6:c.1357C=	ENSP00000359180.2:p.Arg453=
ENST00000370163.7:c.1405C=	ENSP00000359182.3:p.Arg469=
ENST00000370165.7:c.1405C=	ENSP00000359184.3:p.Arg469=
ENST00000477753.1:n.664C=
NM_000028.2:c.1405C=	NP_000019.2:p.Arg469=
NM_000642.2:c.1405C=	NP_000633.2:p.Arg469=
NM_000643.2:c.1405C=	NP_000634.2:p.Arg469=
NM_000644.2:c.1405C=	NP_000635.2:p.Arg469=
NM_000645.2:c.1354C=	NP_000636.2:p.Arg452=
NM_000646.2:c.1357C=	NP_000637.2:p.Arg453=
XM_005270557.1:c.1405C=	XP_005270614.1:p.Arg469=
XM_005270557.2:c.1405C=	XP_005270614.1:p.Arg469=
NM_000642.3:c.1405C= MANE Select	NP_000633.2:p.Arg469=