Canonical Allele Identifier: CA2680762430

Gene: IYD

Linked Data

• gnomAD v4: 6-150398686-CTTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398695_150398698del , CM000668.2:g.150398695_150398698del	GRCh38
NC_000006.11:g.150719831_150719834del , CM000668.1:g.150719831_150719834del	GRCh37
NC_000006.10:g.150761524_150761527del	NCBI36
NG_016007.1:g.34804_34807del
NG_016007.2:g.34804_34807del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*458_*461del MANE Select	ENSP00000343763.4:n.*458_*461del
ENST00000229447.9:c.*558_*561del	ENSP00000229447.5:n.*558_*561del
ENST00000344419.7:c.*458_*461del	ENSP00000343763.3:n.*458_*461del
NM_001164694.1:c.*558_*561del	NP_001158166.1:n.*558_*561del
NM_001164695.1:c.*645_*648del	NP_001158167.1:n.*645_*648del
NM_203395.2:c.*458_*461del	NP_981932.1:n.*458_*461del
NM_001318495.1:c.*458_*461del	NP_001305424.1:n.*458_*461del
NR_134655.1:n.1641_1644del
NM_001164694.2:c.*558_*561del	NP_001158166.1:n.*558_*561del
NM_001164695.2:c.*645_*648del	NP_001158167.1:n.*645_*648del
NM_001318495.2:c.*458_*461del	NP_001305424.1:n.*458_*461del
NM_203395.3:c.*458_*461del MANE Select	NP_981932.1:n.*458_*461del
NR_134655.2:n.1521_1524del