Canonical Allele Identifier: CA2680762402

Gene: IYD

Linked Data

• gnomAD v4: 6-150398638-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398638C>T , CM000668.2:g.150398638C>T	GRCh38
NC_000006.11:g.150719774C>T , CM000668.1:g.150719774C>T	GRCh37
NC_000006.10:g.150761467C>T	NCBI36
NG_016007.1:g.34747C>T
NG_016007.2:g.34747C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*401C>T MANE Select	ENSP00000343763.4:n.*401C>T
ENST00000229447.9:c.*501C>T	ENSP00000229447.5:n.*501C>T
ENST00000344419.7:c.*401C>T	ENSP00000343763.3:n.*401C>T
NM_001164694.1:c.*501C>T	NP_001158166.1:n.*501C>T
NM_001164695.1:c.*588C>T	NP_001158167.1:n.*588C>T
NM_203395.2:c.*401C>T	NP_981932.1:n.*401C>T
NM_001318495.1:c.*401C>T	NP_001305424.1:n.*401C>T
NR_134655.1:n.1584C>T
NM_001164694.2:c.*501C>T	NP_001158166.1:n.*501C>T
NM_001164695.2:c.*588C>T	NP_001158167.1:n.*588C>T
NM_001318495.2:c.*401C>T	NP_001305424.1:n.*401C>T
NM_203395.3:c.*401C>T MANE Select	NP_981932.1:n.*401C>T
NR_134655.2:n.1464C>T