Canonical Allele Identifier: CA1515643509

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438781A= , CM000666.2:g.177438781A=	GRCh38
NC_000004.11:g.178359935A= , CM000666.1:g.178359935A=	GRCh37
NC_000004.10:g.178596929A=	NCBI36
NG_011845.2:g.8723T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.471T= MANE Select	ENSP00000264595.2:p.Asp157=
ENST00000264595.6:c.471T=	ENSP00000264595.2:p.Asp157=
ENST00000502310.5:c.126T=	ENSP00000423798.1:p.Asp42=
ENST00000506853.5:n.505T=
ENST00000510635.1:c.167T=
ENST00000510955.5:n.392T=
NM_000027.3:c.471T=	NP_000018.2:p.Asp157=
NM_001171988.1:c.471T=	NP_001165459.1:p.Asp157=
NR_033655.1:n.599T=
XM_006714123.2:c.471T=	XP_006714186.1:p.Asp157=
XR_001741155.2:n.565T=
NM_000027.4:c.471T= MANE Select	NP_000018.2:p.Asp157=
NM_001171988.2:c.471T=	NP_001165459.1:p.Asp157=
NR_033655.2:n.533T=