Canonical Allele Identifier: CA1515641957

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437494T= , CM000666.2:g.177437494T=	GRCh38
NC_000004.11:g.178358648T= , CM000666.1:g.178358648T=	GRCh37
NC_000004.10:g.178595642T=	NCBI36
NG_011845.2:g.10010A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.533A= MANE Select	ENSP00000264595.2:p.Tyr178=
ENST00000264595.6:c.533A=	ENSP00000264595.2:p.Tyr178=
ENST00000502310.5:c.188A=	ENSP00000423798.1:p.Tyr63=
ENST00000506853.5:n.567A=
ENST00000510635.1:c.229A=
ENST00000510955.5:n.454A=
NM_000027.3:c.533A=	NP_000018.2:p.Tyr178=
NM_001171988.1:c.533A=	NP_001165459.1:p.Tyr178=
NR_033655.1:n.661A=
XM_006714123.2:c.533A=	XP_006714186.1:p.Tyr178=
XR_001741155.2:n.627A=
NM_000027.4:c.533A= MANE Select	NP_000018.2:p.Tyr178=
NM_001171988.2:c.533A=	NP_001165459.1:p.Tyr178=
NR_033655.2:n.595A=