Canonical Allele Identifier: CA1515642062

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437551A= , CM000666.2:g.177437551A=	GRCh38
NC_000004.11:g.178358705A= , CM000666.1:g.178358705A=	GRCh37
NC_000004.10:g.178595699A=	NCBI36
NG_011845.2:g.9953T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.508-32T= MANE Select	ENSP00000264595.2:n.508-32T=
ENST00000264595.6:c.508-32T=	ENSP00000264595.2:n.508-32T=
ENST00000502310.5:c.163-32T=	ENSP00000423798.1:n.163-32T=
ENST00000506853.5:n.542-32T=
ENST00000510635.1:c.204-32T=
ENST00000510955.5:n.429-32T=
NM_000027.3:c.508-32T=	NP_000018.2:n.508-32T=
NM_001171988.1:c.508-32T=	NP_001165459.1:n.508-32T=
NR_033655.1:n.636-32T=
XM_006714123.2:c.508-32T=	XP_006714186.1:n.508-32T=
XR_001741155.2:n.602-32T=
NM_000027.4:c.508-32T= MANE Select	NP_000018.2:n.508-32T=
NM_001171988.2:c.508-32T=	NP_001165459.1:n.508-32T=
NR_033655.2:n.570-32T=