Canonical Allele Identifier: CA1515649251
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442272G= , CM000666.2:g.177442272G= GRCh38
NC_000004.11:g.178363426G= , CM000666.1:g.178363426G= GRCh37
NC_000004.10:g.178600420G= NCBI36
NG_011845.2:g.5232C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.104C= MANE Select ENSP00000264595.2:p.Pro35=
ENST00000264595.6:c.104C= ENSP00000264595.2:p.Pro35=
ENST00000506853.5:n.138C=
ENST00000510955.5:n.138C=
ENST00000511231.1:n.138C=
NM_000027.3:c.104C= NP_000018.2:p.Pro35=
NM_001171988.1:c.104C= NP_001165459.1:p.Pro35=
NR_033655.1:n.232C=
XM_006714123.2:c.104C= XP_006714186.1:p.Pro35=
XR_001741155.2:n.198C=
NM_000027.4:c.104C= MANE Select NP_000018.2:p.Pro35=
NM_001171988.2:c.104C= NP_001165459.1:p.Pro35=
NR_033655.2:n.166C=