Canonical Allele Identifier: CA2680762723

Gene: IYD

Linked Data

• gnomAD v4: 6-150398989-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398989G>A , CM000668.2:g.150398989G>A	GRCh38
NC_000006.11:g.150720125G>A , CM000668.1:g.150720125G>A	GRCh37
NC_000006.10:g.150761818G>A	NCBI36
NG_016007.1:g.35098G>A
NG_016007.2:g.35098G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*752G>A MANE Select	ENSP00000343763.4:n.*752G>A
ENST00000229447.9:c.*852G>A	ENSP00000229447.5:n.*852G>A
ENST00000344419.7:c.*752G>A	ENSP00000343763.3:n.*752G>A
NM_001164694.1:c.*852G>A	NP_001158166.1:n.*852G>A
NM_001164695.1:c.*939G>A	NP_001158167.1:n.*939G>A
NM_203395.2:c.*752G>A	NP_981932.1:n.*752G>A
NM_001318495.1:c.*752G>A	NP_001305424.1:n.*752G>A
NR_134655.1:n.1935G>A
NM_001164694.2:c.*852G>A	NP_001158166.1:n.*852G>A
NM_001164695.2:c.*939G>A	NP_001158167.1:n.*939G>A
NM_001318495.2:c.*752G>A	NP_001305424.1:n.*752G>A
NM_203395.3:c.*752G>A MANE Select	NP_981932.1:n.*752G>A
NR_134655.2:n.1815G>A