Canonical Allele Identifier: CA1515645066
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439733G= , CM000666.2:g.177439733G= GRCh38
NC_000004.11:g.178360887G= , CM000666.1:g.178360887G= GRCh37
NC_000004.10:g.178597881G= NCBI36
NG_011845.2:g.7771C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.282-45C= MANE Select ENSP00000264595.2:n.282-45C=
ENST00000264595.6:c.282-45C= ENSP00000264595.2:n.282-45C=
ENST00000506853.5:n.316-45C=
ENST00000510955.5:n.315+540C=
NM_000027.3:c.282-45C= NP_000018.2:n.282-45C=
NM_001171988.1:c.282-45C= NP_001165459.1:n.282-45C=
NR_033655.1:n.410-45C=
XM_006714123.2:c.282-45C= XP_006714186.1:n.282-45C=
XR_001741155.2:n.376-45C=
NM_000027.4:c.282-45C= MANE Select NP_000018.2:n.282-45C=
NM_001171988.2:c.282-45C= NP_001165459.1:n.282-45C=
NR_033655.2:n.344-45C=