Canonical Allele Identifier: CA150046026

Gene: IYD

Linked Data

• dbSNP Id: rs200663182
• MyVariant Identifiers: chr6:g.150719834_150719835del (hg19) ; chr6:g.150398698_150398699del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398698_150398699del , CM000668.2:g.150398698_150398699del	GRCh38
NC_000006.11:g.150719834_150719835del , CM000668.1:g.150719834_150719835del	GRCh37
NC_000006.10:g.150761527_150761528del	NCBI36
NG_016007.1:g.34807_34808del
NG_016007.2:g.34807_34808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*461_*462del MANE Select	ENSP00000343763.4:n.*461_*462del
ENST00000229447.9:c.*561_*562del	ENSP00000229447.5:n.*561_*562del
ENST00000344419.7:c.*461_*462del	ENSP00000343763.3:n.*461_*462del
NM_001164694.1:c.*561_*562del	NP_001158166.1:n.*561_*562del
NM_001164695.1:c.*648_*649del	NP_001158167.1:n.*648_*649del
NM_203395.2:c.*461_*462del	NP_981932.1:n.*461_*462del
NM_001318495.1:c.*461_*462del	NP_001305424.1:n.*461_*462del
NR_134655.1:n.1644_1645del
NM_001164694.2:c.*561_*562del	NP_001158166.1:n.*561_*562del
NM_001164695.2:c.*648_*649del	NP_001158167.1:n.*648_*649del
NM_001318495.2:c.*461_*462del	NP_001305424.1:n.*461_*462del
NM_203395.3:c.*461_*462del MANE Select	NP_981932.1:n.*461_*462del
NR_134655.2:n.1524_1525del