Canonical Allele Identifier: CA1515648759

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442133G= , CM000666.2:g.177442133G=	GRCh38
NC_000004.11:g.178363287G= , CM000666.1:g.178363287G=	GRCh37
NC_000004.10:g.178600281G=	NCBI36
NG_011845.2:g.5371C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.127+116C= MANE Select	ENSP00000264595.2:n.127+116C=
ENST00000264595.6:c.127+116C=	ENSP00000264595.2:n.127+116C=
ENST00000506853.5:n.161+116C=
ENST00000510955.5:n.161+116C=
ENST00000511231.1:n.161+116C=
NM_000027.3:c.127+116C=	NP_000018.2:n.127+116C=
NM_001171988.1:c.127+116C=	NP_001165459.1:n.127+116C=
NR_033655.1:n.255+116C=
XM_006714123.2:c.127+116C=	XP_006714186.1:n.127+116C=
XR_001741155.2:n.221+116C=
NM_000027.4:c.127+116C= MANE Select	NP_000018.2:n.127+116C=
NM_001171988.2:c.127+116C=	NP_001165459.1:n.127+116C=
NR_033655.2:n.189+116C=