Canonical Allele Identifier: CA1515641911

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437477G= , CM000666.2:g.177437477G=	GRCh38
NC_000004.11:g.178358631G= , CM000666.1:g.178358631G=	GRCh37
NC_000004.10:g.178595625G=	NCBI36
NG_011845.2:g.10027C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.550C= MANE Select	ENSP00000264595.2:p.Pro184=
ENST00000264595.6:c.550C=	ENSP00000264595.2:p.Pro184=
ENST00000502310.5:c.205C=	ENSP00000423798.1:p.Pro69=
ENST00000506853.5:n.584C=
ENST00000510635.1:c.246C=
ENST00000510955.5:n.471C=
NM_000027.3:c.550C=	NP_000018.2:p.Pro184=
NM_001171988.1:c.550C=	NP_001165459.1:p.Pro184=
NR_033655.1:n.678C=
XM_006714123.2:c.550C=	XP_006714186.1:p.Pro184=
XR_001741155.2:n.644C=
NM_000027.4:c.550C= MANE Select	NP_000018.2:p.Pro184=
NM_001171988.2:c.550C=	NP_001165459.1:p.Pro184=
NR_033655.2:n.612C=