Canonical Allele Identifier: CA1515644888
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439659T= , CM000666.2:g.177439659T= GRCh38
NC_000004.11:g.178360813T= , CM000666.1:g.178360813T= GRCh37
NC_000004.10:g.178597807T= NCBI36
NG_011845.2:g.7845A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.311A= MANE Select ENSP00000264595.2:p.Asp104=
ENST00000264595.6:c.311A= ENSP00000264595.2:p.Asp104=
ENST00000506853.5:n.345A=
ENST00000510635.1:c.7A=
ENST00000510955.5:n.315+614A=
NM_000027.3:c.311A= NP_000018.2:p.Asp104=
NM_001171988.1:c.311A= NP_001165459.1:p.Asp104=
NR_033655.1:n.439A=
XM_006714123.2:c.311A= XP_006714186.1:p.Asp104=
XR_001741155.2:n.405A=
NM_000027.4:c.311A= MANE Select NP_000018.2:p.Asp104=
NM_001171988.2:c.311A= NP_001165459.1:p.Asp104=
NR_033655.2:n.373A=