Canonical Allele Identifier: CA1515646329
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177440553T= , CM000666.2:g.177440553T= GRCh38
NC_000004.11:g.178361707T= , CM000666.1:g.178361707T= GRCh37
NC_000004.10:g.178598701T= NCBI36
NG_011845.2:g.6951A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.128-127A= MANE Select ENSP00000264595.2:n.128-127A=
ENST00000264595.6:c.128-127A= ENSP00000264595.2:n.128-127A=
ENST00000506853.5:n.162-127A=
ENST00000510955.5:n.162-127A=
ENST00000511231.1:n.162-127A=
NM_000027.3:c.128-127A= NP_000018.2:n.128-127A=
NM_001171988.1:c.128-127A= NP_001165459.1:n.128-127A=
NR_033655.1:n.256-127A=
XM_006714123.2:c.128-127A= XP_006714186.1:n.128-127A=
XR_001741155.2:n.222-127A=
NM_000027.4:c.128-127A= MANE Select NP_000018.2:n.128-127A=
NM_001171988.2:c.128-127A= NP_001165459.1:n.128-127A=
NR_033655.2:n.190-127A=