Canonical Allele Identifier: CA571090935

Gene: IYD

Linked Data

• dbSNP Id: rs1433198655
• gnomAD v2: 6-150719732-CATG-C
• gnomAD v3: 6-150398596-CATG-C
• gnomAD v4: 6-150398596-CATG-C
• MyVariant Identifiers: chr6:g.150719733_150719735del (hg19) ; chr6:g.150398597_150398599del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398601_150398603del , CM000668.2:g.150398601_150398603del	GRCh38
NC_000006.11:g.150719737_150719739del , CM000668.1:g.150719737_150719739del	GRCh37
NC_000006.10:g.150761430_150761432del	NCBI36
NG_016007.1:g.34710_34712del
NG_016007.2:g.34710_34712del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*364_*366del MANE Select	ENSP00000343763.4:n.*364_*366del
ENST00000229447.9:c.*464_*466del	ENSP00000229447.5:n.*464_*466del
ENST00000344419.7:c.*364_*366del	ENSP00000343763.3:n.*364_*366del
NM_001164694.1:c.*464_*466del	NP_001158166.1:n.*464_*466del
NM_001164695.1:c.*551_*553del	NP_001158167.1:n.*551_*553del
NM_203395.2:c.*364_*366del	NP_981932.1:n.*364_*366del
NM_001318495.1:c.*364_*366del	NP_001305424.1:n.*364_*366del
NR_134655.1:n.1547_1549del
NM_001164694.2:c.*464_*466del	NP_001158166.1:n.*464_*466del
NM_001164695.2:c.*551_*553del	NP_001158167.1:n.*551_*553del
NM_001318495.2:c.*364_*366del	NP_001305424.1:n.*364_*366del
NM_203395.3:c.*364_*366del MANE Select	NP_981932.1:n.*364_*366del
NR_134655.2:n.1427_1429del