Canonical Allele Identifier: CA358782704
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437446A>T , CM000666.2:g.177437446A>T GRCh38
NC_000004.11:g.178358600A>T , CM000666.1:g.178358600A>T GRCh37
NC_000004.10:g.178595594A>T NCBI36
NG_011845.2:g.10058T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.581T>A MANE Select ENSP00000264595.2:p.Ile194Asn
ENST00000264595.6:c.581T>A ENSP00000264595.2:p.Ile194Asn
ENST00000502310.5:c.236T>A ENSP00000423798.1:p.Ile79Asn
ENST00000506853.5:n.615T>A
ENST00000510635.1:c.277T>A
ENST00000510955.5:n.502T>A
NM_000027.3:c.581T>A NP_000018.2:p.Ile194Asn
NM_001171988.1:c.581T>A NP_001165459.1:p.Ile194Asn
NR_033655.1:n.709T>A
XM_006714123.2:c.581T>A XP_006714186.1:p.Ile194Asn
XR_001741155.2:n.675T>A
NM_000027.4:c.581T>A MANE Select NP_000018.2:p.Ile194Asn
NM_001171988.2:c.581T>A NP_001165459.1:p.Ile194Asn
NR_033655.2:n.643T>A