Canonical Allele Identifier: CA1515649274
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442281T= , CM000666.2:g.177442281T= GRCh38
NC_000004.11:g.178363435T= , CM000666.1:g.178363435T= GRCh37
NC_000004.10:g.178600429T= NCBI36
NG_011845.2:g.5223A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.95A= MANE Select ENSP00000264595.2:p.Asn32=
ENST00000264595.6:c.95A= ENSP00000264595.2:p.Asn32=
ENST00000506853.5:n.129A=
ENST00000510955.5:n.129A=
ENST00000511231.1:n.129A=
NM_000027.3:c.95A= NP_000018.2:p.Asn32=
NM_001171988.1:c.95A= NP_001165459.1:p.Asn32=
NR_033655.1:n.223A=
XM_006714123.2:c.95A= XP_006714186.1:p.Asn32=
XR_001741155.2:n.189A=
NM_000027.4:c.95A= MANE Select NP_000018.2:p.Asn32=
NM_001171988.2:c.95A= NP_001165459.1:p.Asn32=
NR_033655.2:n.157A=