Canonical Allele Identifier: CA2680762837

Gene: IYD

Linked Data

• gnomAD v4: 6-150399065-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399066_150399067del , CM000668.2:g.150399066_150399067del	GRCh38
NC_000006.11:g.150720202_150720203del , CM000668.1:g.150720202_150720203del	GRCh37
NC_000006.10:g.150761895_150761896del	NCBI36
NG_016007.1:g.35175_35176del
NG_016007.2:g.35175_35176del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*829_*830del MANE Select	ENSP00000343763.4:n.*829_*830del
ENST00000229447.9:c.*929_*930del	ENSP00000229447.5:n.*929_*930del
ENST00000344419.7:c.*829_*830del	ENSP00000343763.3:n.*829_*830del
NM_001164694.1:c.*929_*930del	NP_001158166.1:n.*929_*930del
NM_001164695.1:c.*1016_*1017del	NP_001158167.1:n.*1016_*1017del
NM_203395.2:c.*829_*830del	NP_981932.1:n.*829_*830del
NM_001318495.1:c.*829_*830del	NP_001305424.1:n.*829_*830del
NR_134655.1:n.2012_2013del
NM_001164694.2:c.*929_*930del	NP_001158166.1:n.*929_*930del
NM_001164695.2:c.*1016_*1017del	NP_001158167.1:n.*1016_*1017del
NM_001318495.2:c.*829_*830del	NP_001305424.1:n.*829_*830del
NM_203395.3:c.*829_*830del MANE Select	NP_981932.1:n.*829_*830del
NR_134655.2:n.1892_1893del