Canonical Allele Identifier: CA1515649463
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442342C= , CM000666.2:g.177442342C= GRCh38
NC_000004.11:g.178363496C= , CM000666.1:g.178363496C= GRCh37
NC_000004.10:g.178600490C= NCBI36
NG_011845.2:g.5162G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.34G= MANE Select ENSP00000264595.2:p.Val12=
ENST00000264595.6:c.34G= ENSP00000264595.2:p.Val12=
ENST00000506853.5:n.68G=
ENST00000510955.5:n.68G=
ENST00000511231.1:n.68G=
NM_000027.3:c.34G= NP_000018.2:p.Val12=
NM_001171988.1:c.34G= NP_001165459.1:p.Val12=
NR_033655.1:n.162G=
XM_006714123.2:c.34G= XP_006714186.1:p.Val12=
XR_001741155.2:n.128G=
NM_000027.4:c.34G= MANE Select NP_000018.2:p.Val12=
NM_001171988.2:c.34G= NP_001165459.1:p.Val12=
NR_033655.2:n.96G=