Canonical Allele Identifier: CA358783718
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439642T>A , CM000666.2:g.177439642T>A GRCh38
NC_000004.11:g.178360796T>A , CM000666.1:g.178360796T>A GRCh37
NC_000004.10:g.178597790T>A NCBI36
NG_011845.2:g.7862A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.328A>T MANE Select ENSP00000264595.2:p.Asn110Tyr
ENST00000264595.6:c.328A>T ENSP00000264595.2:p.Asn110Tyr
ENST00000506853.5:n.362A>T
ENST00000510635.1:c.24A>T
ENST00000510955.5:n.315+631A>T
NM_000027.3:c.328A>T NP_000018.2:p.Asn110Tyr
NM_001171988.1:c.328A>T NP_001165459.1:p.Asn110Tyr
NR_033655.1:n.456A>T
XM_006714123.2:c.328A>T XP_006714186.1:p.Asn110Tyr
XR_001741155.2:n.422A>T
NM_000027.4:c.328A>T MANE Select NP_000018.2:p.Asn110Tyr
NM_001171988.2:c.328A>T NP_001165459.1:p.Asn110Tyr
NR_033655.2:n.390A>T