Canonical Allele Identifier: CA1515649339
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442301G= , CM000666.2:g.177442301G= GRCh38
NC_000004.11:g.178363455G= , CM000666.1:g.178363455G= GRCh37
NC_000004.10:g.178600449G= NCBI36
NG_011845.2:g.5203C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.75C= MANE Select ENSP00000264595.2:p.Ser25=
ENST00000264595.6:c.75C= ENSP00000264595.2:p.Ser25=
ENST00000506853.5:n.109C=
ENST00000510955.5:n.109C=
ENST00000511231.1:n.109C=
NM_000027.3:c.75C= NP_000018.2:p.Ser25=
NM_001171988.1:c.75C= NP_001165459.1:p.Ser25=
NR_033655.1:n.203C=
XM_006714123.2:c.75C= XP_006714186.1:p.Ser25=
XR_001741155.2:n.169C=
NM_000027.4:c.75C= MANE Select NP_000018.2:p.Ser25=
NM_001171988.2:c.75C= NP_001165459.1:p.Ser25=
NR_033655.2:n.137C=