Canonical Allele Identifier: CA2531512741
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439186T>G , CM000666.2:g.177439186T>G GRCh38
NC_000004.11:g.178360340T>G , CM000666.1:g.178360340T>G GRCh37
NC_000004.10:g.178597334T>G NCBI36
NG_011845.2:g.8318A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.395-329A>C MANE Select ENSP00000264595.2:n.395-329A>C
ENST00000264595.6:c.395-329A>C ENSP00000264595.2:n.395-329A>C
ENST00000502310.5:c.50-329A>C ENSP00000423798.1:n.50-329A>C
ENST00000506853.5:n.429-329A>C
ENST00000510635.1:c.91-329A>C
ENST00000510955.5:n.316-329A>C
NM_000027.3:c.395-329A>C NP_000018.2:n.395-329A>C
NM_001171988.1:c.395-329A>C NP_001165459.1:n.395-329A>C
NR_033655.1:n.523-329A>C
XM_006714123.2:c.395-329A>C XP_006714186.1:n.395-329A>C
XR_001741155.2:n.489-329A>C
NM_000027.4:c.395-329A>C MANE Select NP_000018.2:n.395-329A>C
NM_001171988.2:c.395-329A>C NP_001165459.1:n.395-329A>C
NR_033655.2:n.457-329A>C