Canonical Allele Identifier: CA2680762433
Gene: IYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398704del , CM000668.2:g.150398704del GRCh38
NC_000006.11:g.150719840del , CM000668.1:g.150719840del GRCh37
NC_000006.10:g.150761533del NCBI36
NG_016007.1:g.34813del
NG_016007.2:g.34813del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*467del MANE Select ENSP00000343763.4:n.*467del
ENST00000229447.9:c.*567del ENSP00000229447.5:n.*567del
ENST00000344419.7:c.*467del ENSP00000343763.3:n.*467del
NM_001164694.1:c.*567del NP_001158166.1:n.*567del
NM_001164695.1:c.*654del NP_001158167.1:n.*654del
NM_203395.2:c.*467del NP_981932.1:n.*467del
NM_001318495.1:c.*467del NP_001305424.1:n.*467del
NR_134655.1:n.1650del
NM_001164694.2:c.*567del NP_001158166.1:n.*567del
NM_001164695.2:c.*654del NP_001158167.1:n.*654del
NM_001318495.2:c.*467del NP_001305424.1:n.*467del
NM_203395.3:c.*467del MANE Select NP_981932.1:n.*467del
NR_134655.2:n.1530del