Canonical Allele Identifier: CA1515641905

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437474G= , CM000666.2:g.177437474G=	GRCh38
NC_000004.11:g.178358628G= , CM000666.1:g.178358628G=	GRCh37
NC_000004.10:g.178595622G=	NCBI36
NG_011845.2:g.10030C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.553C= MANE Select	ENSP00000264595.2:p.Pro185=
ENST00000264595.6:c.553C=	ENSP00000264595.2:p.Pro185=
ENST00000502310.5:c.208C=	ENSP00000423798.1:p.Pro70=
ENST00000506853.5:n.587C=
ENST00000510635.1:c.249C=
ENST00000510955.5:n.474C=
NM_000027.3:c.553C=	NP_000018.2:p.Pro185=
NM_001171988.1:c.553C=	NP_001165459.1:p.Pro185=
NR_033655.1:n.681C=
XM_006714123.2:c.553C=	XP_006714186.1:p.Pro185=
XR_001741155.2:n.647C=
NM_000027.4:c.553C= MANE Select	NP_000018.2:p.Pro185=
NM_001171988.2:c.553C=	NP_001165459.1:p.Pro185=
NR_033655.2:n.615C=