Canonical Allele Identifier: CA1515641970

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437503G= , CM000666.2:g.177437503G=	GRCh38
NC_000004.11:g.178358657G= , CM000666.1:g.178358657G=	GRCh37
NC_000004.10:g.178595651G=	NCBI36
NG_011845.2:g.10001C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.524C= MANE Select	ENSP00000264595.2:p.Pro175=
ENST00000264595.6:c.524C=	ENSP00000264595.2:p.Pro175=
ENST00000502310.5:c.179C=	ENSP00000423798.1:p.Pro60=
ENST00000506853.5:n.558C=
ENST00000510635.1:c.220C=
ENST00000510955.5:n.445C=
NM_000027.3:c.524C=	NP_000018.2:p.Pro175=
NM_001171988.1:c.524C=	NP_001165459.1:p.Pro175=
NR_033655.1:n.652C=
XM_006714123.2:c.524C=	XP_006714186.1:p.Pro175=
XR_001741155.2:n.618C=
NM_000027.4:c.524C= MANE Select	NP_000018.2:p.Pro175=
NM_001171988.2:c.524C=	NP_001165459.1:p.Pro175=
NR_033655.2:n.586C=