Canonical Allele Identifier: CA1515644844
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439641T= , CM000666.2:g.177439641T= GRCh38
NC_000004.11:g.178360795T= , CM000666.1:g.178360795T= GRCh37
NC_000004.10:g.178597789T= NCBI36
NG_011845.2:g.7863A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.329A= MANE Select ENSP00000264595.2:p.Asn110=
ENST00000264595.6:c.329A= ENSP00000264595.2:p.Asn110=
ENST00000506853.5:n.363A=
ENST00000510635.1:c.25A=
ENST00000510955.5:n.315+632A=
NM_000027.3:c.329A= NP_000018.2:p.Asn110=
NM_001171988.1:c.329A= NP_001165459.1:p.Asn110=
NR_033655.1:n.457A=
XM_006714123.2:c.329A= XP_006714186.1:p.Asn110=
XR_001741155.2:n.423A=
NM_000027.4:c.329A= MANE Select NP_000018.2:p.Asn110=
NM_001171988.2:c.329A= NP_001165459.1:p.Asn110=
NR_033655.2:n.391A=