Canonical Allele Identifier: CA1515646169

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177440458T= , CM000666.2:g.177440458T=	GRCh38
NC_000004.11:g.178361612T= , CM000666.1:g.178361612T=	GRCh37
NC_000004.10:g.178598606T=	NCBI36
NG_011845.2:g.7046A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.128-32A= MANE Select	ENSP00000264595.2:n.128-32A=
ENST00000264595.6:c.128-32A=	ENSP00000264595.2:n.128-32A=
ENST00000506853.5:n.162-32A=
ENST00000510955.5:n.162-32A=
ENST00000511231.1:n.162-32A=
NM_000027.3:c.128-32A=	NP_000018.2:n.128-32A=
NM_001171988.1:c.128-32A=	NP_001165459.1:n.128-32A=
NR_033655.1:n.256-32A=
XM_006714123.2:c.128-32A=	XP_006714186.1:n.128-32A=
XR_001741155.2:n.222-32A=
NM_000027.4:c.128-32A= MANE Select	NP_000018.2:n.128-32A=
NM_001171988.2:c.128-32A=	NP_001165459.1:n.128-32A=
NR_033655.2:n.190-32A=