Canonical Allele Identifier: CA150046034

Gene: IYD

Linked Data

• dbSNP Id: rs1491352606
• gnomAD v2: 6-150719834-T-TA
• gnomAD v3: 6-150398698-T-TA
• gnomAD v4: 6-150398698-T-TA
• MyVariant Identifiers: chr6:g.150719834_150719835insA (hg19) ; chr6:g.150398698_150398699insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398699dup , CM000668.2:g.150398699dup	GRCh38
NC_000006.11:g.150719835dup , CM000668.1:g.150719835dup	GRCh37
NC_000006.10:g.150761528dup	NCBI36
NG_016007.1:g.34808dup
NG_016007.2:g.34808dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*462dup MANE Select	ENSP00000343763.4:n.*462dup
ENST00000229447.9:c.*562dup	ENSP00000229447.5:n.*562dup
ENST00000344419.7:c.*462dup	ENSP00000343763.3:n.*462dup
NM_001164694.1:c.*562dup	NP_001158166.1:n.*562dup
NM_001164695.1:c.*649dup	NP_001158167.1:n.*649dup
NM_203395.2:c.*462dup	NP_981932.1:n.*462dup
NM_001318495.1:c.*462dup	NP_001305424.1:n.*462dup
NR_134655.1:n.1645dup
NM_001164694.2:c.*562dup	NP_001158166.1:n.*562dup
NM_001164695.2:c.*649dup	NP_001158167.1:n.*649dup
NM_001318495.2:c.*462dup	NP_001305424.1:n.*462dup
NM_203395.3:c.*462dup MANE Select	NP_981932.1:n.*462dup
NR_134655.2:n.1525dup