Canonical Allele Identifier: CA1515637606
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434422C= , CM000666.2:g.177434422C= GRCh38
NC_000004.11:g.178355576C= , CM000666.1:g.178355576C= GRCh37
NC_000004.10:g.178592570C= NCBI36
NG_011845.2:g.13082G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.766G= MANE Select ENSP00000264595.2:p.Ala256=
ENST00000264595.6:c.766G= ENSP00000264595.2:p.Ala256=
ENST00000502310.5:c.337G= ENSP00000423798.1:p.Ala113=
ENST00000506853.5:n.724G=
NM_000027.3:c.766G= NP_000018.2:p.Ala256=
NM_001171988.1:c.736G= NP_001165459.1:p.Ala246=
NR_033655.1:n.818G=
XM_006714123.2:c.*60G= XP_006714186.1:n.*60G=
XR_001741155.2:n.838G=
NM_000027.4:c.766G= MANE Select NP_000018.2:p.Ala256=
NM_001171988.2:c.736G= NP_001165459.1:p.Ala246=
NR_033655.2:n.752G=