Canonical Allele Identifier: CA1515645925
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177440344G= , CM000666.2:g.177440344G= GRCh38
NC_000004.11:g.178361498G= , CM000666.1:g.178361498G= GRCh37
NC_000004.10:g.178598492G= NCBI36
NG_011845.2:g.7160C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.210C= MANE Select ENSP00000264595.2:p.Asp70=
ENST00000264595.6:c.210C= ENSP00000264595.2:p.Asp70=
ENST00000506853.5:n.244C=
ENST00000510955.5:n.244C=
ENST00000511231.1:n.244C=
NM_000027.3:c.210C= NP_000018.2:p.Asp70=
NM_001171988.1:c.210C= NP_001165459.1:p.Asp70=
NR_033655.1:n.338C=
XM_006714123.2:c.210C= XP_006714186.1:p.Asp70=
XR_001741155.2:n.304C=
NM_000027.4:c.210C= MANE Select NP_000018.2:p.Asp70=
NM_001171988.2:c.210C= NP_001165459.1:p.Asp70=
NR_033655.2:n.272C=