Canonical Allele Identifier: CA2764653779
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439488T>A , CM000666.2:g.177439488T>A GRCh38
NC_000004.11:g.178360642T>A , CM000666.1:g.178360642T>A GRCh37
NC_000004.10:g.178597636T>A NCBI36
NG_011845.2:g.8016A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.394+88A>T MANE Select ENSP00000264595.2:n.394+88A>T
ENST00000264595.6:c.394+88A>T ENSP00000264595.2:n.394+88A>T
ENST00000502310.5:c.49+88A>T ENSP00000423798.1:n.49+88A>T
ENST00000506853.5:n.428+88A>T
ENST00000510635.1:c.90+88A>T
ENST00000510955.5:n.316-631A>T
NM_000027.3:c.394+88A>T NP_000018.2:n.394+88A>T
NM_001171988.1:c.394+88A>T NP_001165459.1:n.394+88A>T
NR_033655.1:n.522+88A>T
XM_006714123.2:c.394+88A>T XP_006714186.1:n.394+88A>T
XR_001741155.2:n.488+88A>T
NM_000027.4:c.394+88A>T MANE Select NP_000018.2:n.394+88A>T
NM_001171988.2:c.394+88A>T NP_001165459.1:n.394+88A>T
NR_033655.2:n.456+88A>T