Canonical Allele Identifier: CA1515646384
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177440613G= , CM000666.2:g.177440613G= GRCh38
NC_000004.11:g.178361767G= , CM000666.1:g.178361767G= GRCh37
NC_000004.10:g.178598761G= NCBI36
NG_011845.2:g.6891C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.128-187C= MANE Select ENSP00000264595.2:n.128-187C=
ENST00000264595.6:c.128-187C= ENSP00000264595.2:n.128-187C=
ENST00000506853.5:n.162-187C=
ENST00000510955.5:n.162-187C=
ENST00000511231.1:n.162-187C=
NM_000027.3:c.128-187C= NP_000018.2:n.128-187C=
NM_001171988.1:c.128-187C= NP_001165459.1:n.128-187C=
NR_033655.1:n.256-187C=
XM_006714123.2:c.128-187C= XP_006714186.1:n.128-187C=
XR_001741155.2:n.222-187C=
NM_000027.4:c.128-187C= MANE Select NP_000018.2:n.128-187C=
NM_001171988.2:c.128-187C= NP_001165459.1:n.128-187C=
NR_033655.2:n.190-187C=