Canonical Allele Identifier: CA1672406216

Gene: IYD

Linked Data

• dbSNP Id: rs1778428279

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399062T>G , CM000668.2:g.150399062T>G	GRCh38
NC_000006.11:g.150720198T>G , CM000668.1:g.150720198T>G	GRCh37
NC_000006.10:g.150761891T>G	NCBI36
NG_016007.1:g.35171T>G
NG_016007.2:g.35171T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*825T>G MANE Select	ENSP00000343763.4:n.*825T>G
ENST00000229447.9:c.*925T>G	ENSP00000229447.5:n.*925T>G
ENST00000344419.7:c.*825T>G	ENSP00000343763.3:n.*825T>G
NM_001164694.1:c.*925T>G	NP_001158166.1:n.*925T>G
NM_001164695.1:c.*1012T>G	NP_001158167.1:n.*1012T>G
NM_203395.2:c.*825T>G	NP_981932.1:n.*825T>G
NM_001318495.1:c.*825T>G	NP_001305424.1:n.*825T>G
NR_134655.1:n.2008T>G
NM_001164694.2:c.*925T>G	NP_001158166.1:n.*925T>G
NM_001164695.2:c.*1012T>G	NP_001158167.1:n.*1012T>G
NM_001318495.2:c.*825T>G	NP_001305424.1:n.*825T>G
NM_203395.3:c.*825T>G MANE Select	NP_981932.1:n.*825T>G
NR_134655.2:n.1888T>G