Canonical Allele Identifier: CA1515641794
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437412G= , CM000666.2:g.177437412G= GRCh38
NC_000004.11:g.178358566G= , CM000666.1:g.178358566G= GRCh37
NC_000004.10:g.178595560G= NCBI36
NG_011845.2:g.10092C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.615C= MANE Select ENSP00000264595.2:p.Asp205=
ENST00000264595.6:c.615C= ENSP00000264595.2:p.Asp205=
ENST00000502310.5:c.270C= ENSP00000423798.1:p.Asp90=
ENST00000506853.5:n.649C=
ENST00000510635.1:c.311C=
ENST00000510955.5:n.536C=
NM_000027.3:c.615C= NP_000018.2:p.Asp205=
NM_001171988.1:c.615C= NP_001165459.1:p.Asp205=
NR_033655.1:n.743C=
XM_006714123.2:c.615C= XP_006714186.1:p.Asp205=
XR_001741155.2:n.709C=
NM_000027.4:c.615C= MANE Select NP_000018.2:p.Asp205=
NM_001171988.2:c.615C= NP_001165459.1:p.Asp205=
NR_033655.2:n.677C=