Canonical Allele Identifier: CA1515643686
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177438865T= , CM000666.2:g.177438865T= GRCh38
NC_000004.11:g.178360019T= , CM000666.1:g.178360019T= GRCh37
NC_000004.10:g.178597013T= NCBI36
NG_011845.2:g.8639A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.395-8A= MANE Select ENSP00000264595.2:n.395-8A=
ENST00000264595.6:c.395-8A= ENSP00000264595.2:n.395-8A=
ENST00000502310.5:c.50-8A= ENSP00000423798.1:n.50-8A=
ENST00000506853.5:n.429-8A=
ENST00000510635.1:c.91-8A=
ENST00000510955.5:n.316-8A=
NM_000027.3:c.395-8A= NP_000018.2:n.395-8A=
NM_001171988.1:c.395-8A= NP_001165459.1:n.395-8A=
NR_033655.1:n.523-8A=
XM_006714123.2:c.395-8A= XP_006714186.1:n.395-8A=
XR_001741155.2:n.489-8A=
NM_000027.4:c.395-8A= MANE Select NP_000018.2:n.395-8A=
NM_001171988.2:c.395-8A= NP_001165459.1:n.395-8A=
NR_033655.2:n.457-8A=