Canonical Allele Identifier: CA1515645929
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177440345T= , CM000666.2:g.177440345T= GRCh38
NC_000004.11:g.178361499T= , CM000666.1:g.178361499T= GRCh37
NC_000004.10:g.178598493T= NCBI36
NG_011845.2:g.7159A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.209A= MANE Select ENSP00000264595.2:p.Asp70=
ENST00000264595.6:c.209A= ENSP00000264595.2:p.Asp70=
ENST00000506853.5:n.243A=
ENST00000510955.5:n.243A=
ENST00000511231.1:n.243A=
NM_000027.3:c.209A= NP_000018.2:p.Asp70=
NM_001171988.1:c.209A= NP_001165459.1:p.Asp70=
NR_033655.1:n.337A=
XM_006714123.2:c.209A= XP_006714186.1:p.Asp70=
XR_001741155.2:n.303A=
NM_000027.4:c.209A= MANE Select NP_000018.2:p.Asp70=
NM_001171988.2:c.209A= NP_001165459.1:p.Asp70=
NR_033655.2:n.271A=