Canonical Allele Identifier: CA2672747640
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177438879del , CM000666.2:g.177438879del GRCh38
NC_000004.11:g.178360033del , CM000666.1:g.178360033del GRCh37
NC_000004.10:g.178597027del NCBI36
NG_011845.2:g.8627del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.395-20del MANE Select ENSP00000264595.2:n.395-20del
ENST00000264595.6:c.395-20del ENSP00000264595.2:n.395-20del
ENST00000502310.5:c.50-20del ENSP00000423798.1:n.50-20del
ENST00000506853.5:n.429-20del
ENST00000510635.1:c.91-20del
ENST00000510955.5:n.316-20del
NM_000027.3:c.395-20del NP_000018.2:n.395-20del
NM_001171988.1:c.395-20del NP_001165459.1:n.395-20del
NR_033655.1:n.523-20del
XM_006714123.2:c.395-20del XP_006714186.1:n.395-20del
XR_001741155.2:n.489-20del
NM_000027.4:c.395-20del MANE Select NP_000018.2:n.395-20del
NM_001171988.2:c.395-20del NP_001165459.1:n.395-20del
NR_033655.2:n.457-20del