Canonical Allele Identifier: CA1515649568

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442354G= , CM000666.2:g.177442354G=	GRCh38
NC_000004.11:g.178363508G= , CM000666.1:g.178363508G=	GRCh37
NC_000004.10:g.178600502G=	NCBI36
NG_011845.2:g.5150C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.22C= MANE Select	ENSP00000264595.2:p.Pro8=
ENST00000264595.6:c.22C=	ENSP00000264595.2:p.Pro8=
ENST00000506853.5:n.56C=
ENST00000510955.5:n.56C=
ENST00000511231.1:n.56C=
NM_000027.3:c.22C=	NP_000018.2:p.Pro8=
NM_001171988.1:c.22C=	NP_001165459.1:p.Pro8=
NR_033655.1:n.150C=
XM_006714123.2:c.22C=	XP_006714186.1:p.Pro8=
XR_001741155.2:n.116C=
NM_000027.4:c.22C= MANE Select	NP_000018.2:p.Pro8=
NM_001171988.2:c.22C=	NP_001165459.1:p.Pro8=
NR_033655.2:n.84C=