Canonical Allele Identifier: CA1515644474
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439472G= , CM000666.2:g.177439472G= GRCh38
NC_000004.11:g.178360626G= , CM000666.1:g.178360626G= GRCh37
NC_000004.10:g.178597620G= NCBI36
NG_011845.2:g.8032C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.394+104C= MANE Select ENSP00000264595.2:n.394+104C=
ENST00000264595.6:c.394+104C= ENSP00000264595.2:n.394+104C=
ENST00000502310.5:c.49+104C= ENSP00000423798.1:n.49+104C=
ENST00000506853.5:n.428+104C=
ENST00000510635.1:c.90+104C=
ENST00000510955.5:n.316-615C=
NM_000027.3:c.394+104C= NP_000018.2:n.394+104C=
NM_001171988.1:c.394+104C= NP_001165459.1:n.394+104C=
NR_033655.1:n.522+104C=
XM_006714123.2:c.394+104C= XP_006714186.1:n.394+104C=
XR_001741155.2:n.488+104C=
NM_000027.4:c.394+104C= MANE Select NP_000018.2:n.394+104C=
NM_001171988.2:c.394+104C= NP_001165459.1:n.394+104C=
NR_033655.2:n.456+104C=