Canonical Allele Identifier: CA1515646552

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177440693G= , CM000666.2:g.177440693G=	GRCh38
NC_000004.11:g.178361847G= , CM000666.1:g.178361847G=	GRCh37
NC_000004.10:g.178598841G=	NCBI36
NG_011845.2:g.6811C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.128-267C= MANE Select	ENSP00000264595.2:n.128-267C=
ENST00000264595.6:c.128-267C=	ENSP00000264595.2:n.128-267C=
ENST00000506853.5:n.162-267C=
ENST00000510955.5:n.162-267C=
ENST00000511231.1:n.162-267C=
NM_000027.3:c.128-267C=	NP_000018.2:n.128-267C=
NM_001171988.1:c.128-267C=	NP_001165459.1:n.128-267C=
NR_033655.1:n.256-267C=
XM_006714123.2:c.128-267C=	XP_006714186.1:n.128-267C=
XR_001741155.2:n.222-267C=
NM_000027.4:c.128-267C= MANE Select	NP_000018.2:n.128-267C=
NM_001171988.2:c.128-267C=	NP_001165459.1:n.128-267C=
NR_033655.2:n.190-267C=