Canonical Allele Identifier: CA150046213

Gene: IYD

Linked Data

• dbSNP Id: rs201924267
• MyVariant Identifiers: chr6:g.150720043_150720047del (hg19) ; chr6:g.150398907_150398911del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398907_150398911del , CM000668.2:g.150398907_150398911del	GRCh38
NC_000006.11:g.150720043_150720047del , CM000668.1:g.150720043_150720047del	GRCh37
NC_000006.10:g.150761736_150761740del	NCBI36
NG_016007.1:g.35016_35020del
NG_016007.2:g.35016_35020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*670_*674del MANE Select	ENSP00000343763.4:n.*670_*674del
ENST00000229447.9:c.*770_*774del	ENSP00000229447.5:n.*770_*774del
ENST00000344419.7:c.*670_*674del	ENSP00000343763.3:n.*670_*674del
NM_001164694.1:c.*770_*774del	NP_001158166.1:n.*770_*774del
NM_001164695.1:c.*857_*861del	NP_001158167.1:n.*857_*861del
NM_203395.2:c.*670_*674del	NP_981932.1:n.*670_*674del
NM_001318495.1:c.*670_*674del	NP_001305424.1:n.*670_*674del
NR_134655.1:n.1853_1857del
NM_001164694.2:c.*770_*774del	NP_001158166.1:n.*770_*774del
NM_001164695.2:c.*857_*861del	NP_001158167.1:n.*857_*861del
NM_001318495.2:c.*670_*674del	NP_001305424.1:n.*670_*674del
NM_203395.3:c.*670_*674del MANE Select	NP_981932.1:n.*670_*674del
NR_134655.2:n.1733_1737del