Canonical Allele Identifier: CA1515637637
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434430G= , CM000666.2:g.177434430G= GRCh38
NC_000004.11:g.178355584G= , CM000666.1:g.178355584G= GRCh37
NC_000004.10:g.178592578G= NCBI36
NG_011845.2:g.13074C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.758C= MANE Select ENSP00000264595.2:p.Ala253=
ENST00000264595.6:c.758C= ENSP00000264595.2:p.Ala253=
ENST00000502310.5:c.329C= ENSP00000423798.1:p.Ala110=
ENST00000506853.5:n.716C=
NM_000027.3:c.758C= NP_000018.2:p.Ala253=
NM_001171988.1:c.728C= NP_001165459.1:p.Ala243=
NR_033655.1:n.810C=
XM_006714123.2:c.*52C= XP_006714186.1:n.*52C=
XR_001741155.2:n.830C=
NM_000027.4:c.758C= MANE Select NP_000018.2:p.Ala253=
NM_001171988.2:c.728C= NP_001165459.1:p.Ala243=
NR_033655.2:n.744C=