Canonical Allele Identifier: CA1095800307

Gene: IYD

Linked Data

• dbSNP Id: rs1778422056
• gnomAD v3: 6-150398840-G-A
• gnomAD v4: 6-150398840-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398840G>A , CM000668.2:g.150398840G>A	GRCh38
NC_000006.11:g.150719976G>A , CM000668.1:g.150719976G>A	GRCh37
NC_000006.10:g.150761669G>A	NCBI36
NG_016007.1:g.34949G>A
NG_016007.2:g.34949G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*603G>A MANE Select	ENSP00000343763.4:n.*603G>A
ENST00000229447.9:c.*703G>A	ENSP00000229447.5:n.*703G>A
ENST00000344419.7:c.*603G>A	ENSP00000343763.3:n.*603G>A
NM_001164694.1:c.*703G>A	NP_001158166.1:n.*703G>A
NM_001164695.1:c.*790G>A	NP_001158167.1:n.*790G>A
NM_203395.2:c.*603G>A	NP_981932.1:n.*603G>A
NM_001318495.1:c.*603G>A	NP_001305424.1:n.*603G>A
NR_134655.1:n.1786G>A
NM_001164694.2:c.*703G>A	NP_001158166.1:n.*703G>A
NM_001164695.2:c.*790G>A	NP_001158167.1:n.*790G>A
NM_001318495.2:c.*603G>A	NP_001305424.1:n.*603G>A
NM_203395.3:c.*603G>A MANE Select	NP_981932.1:n.*603G>A
NR_134655.2:n.1666G>A