Canonical Allele Identifier: CA2680762429

Gene: IYD

Linked Data

• gnomAD v4: 6-150398686-C-CTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398696_150398698dup , CM000668.2:g.150398696_150398698dup	GRCh38
NC_000006.11:g.150719832_150719834dup , CM000668.1:g.150719832_150719834dup	GRCh37
NC_000006.10:g.150761525_150761527dup	NCBI36
NG_016007.1:g.34805_34807dup
NG_016007.2:g.34805_34807dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*459_*461dup MANE Select	ENSP00000343763.4:n.*459_*461dup
ENST00000229447.9:c.*559_*561dup	ENSP00000229447.5:n.*559_*561dup
ENST00000344419.7:c.*459_*461dup	ENSP00000343763.3:n.*459_*461dup
NM_001164694.1:c.*559_*561dup	NP_001158166.1:n.*559_*561dup
NM_001164695.1:c.*646_*648dup	NP_001158167.1:n.*646_*648dup
NM_203395.2:c.*459_*461dup	NP_981932.1:n.*459_*461dup
NM_001318495.1:c.*459_*461dup	NP_001305424.1:n.*459_*461dup
NR_134655.1:n.1642_1644dup
NM_001164694.2:c.*559_*561dup	NP_001158166.1:n.*559_*561dup
NM_001164695.2:c.*646_*648dup	NP_001158167.1:n.*646_*648dup
NM_001318495.2:c.*459_*461dup	NP_001305424.1:n.*459_*461dup
NM_203395.3:c.*459_*461dup MANE Select	NP_981932.1:n.*459_*461dup
NR_134655.2:n.1522_1524dup