Canonical Allele Identifier: CA2680762399

Gene: IYD

Linked Data

• gnomAD v4: 6-150398634-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398637_150398639del , CM000668.2:g.150398637_150398639del	GRCh38
NC_000006.11:g.150719773_150719775del , CM000668.1:g.150719773_150719775del	GRCh37
NC_000006.10:g.150761466_150761468del	NCBI36
NG_016007.1:g.34746_34748del
NG_016007.2:g.34746_34748del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*400_*402del MANE Select	ENSP00000343763.4:n.*400_*402del
ENST00000229447.9:c.*500_*502del	ENSP00000229447.5:n.*500_*502del
ENST00000344419.7:c.*400_*402del	ENSP00000343763.3:n.*400_*402del
NM_001164694.1:c.*500_*502del	NP_001158166.1:n.*500_*502del
NM_001164695.1:c.*587_*589del	NP_001158167.1:n.*587_*589del
NM_203395.2:c.*400_*402del	NP_981932.1:n.*400_*402del
NM_001318495.1:c.*400_*402del	NP_001305424.1:n.*400_*402del
NR_134655.1:n.1583_1585del
NM_001164694.2:c.*500_*502del	NP_001158166.1:n.*500_*502del
NM_001164695.2:c.*587_*589del	NP_001158167.1:n.*587_*589del
NM_001318495.2:c.*400_*402del	NP_001305424.1:n.*400_*402del
NM_203395.3:c.*400_*402del MANE Select	NP_981932.1:n.*400_*402del
NR_134655.2:n.1463_1465del