Canonical Allele Identifier: CA1672405988
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398581C= , CM000668.2:g.150398581C= GRCh38
NC_000006.11:g.150719717C= , CM000668.1:g.150719717C= GRCh37
NC_000006.10:g.150761410C= NCBI36
NG_016007.1:g.34690C=
NG_016007.2:g.34690C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*344C= MANE Select ENSP00000343763.4:n.*344C=
ENST00000229447.9:c.*444C= ENSP00000229447.5:n.*444C=
ENST00000344419.7:c.*344C= ENSP00000343763.3:n.*344C=
NM_001164694.1:c.*444C= NP_001158166.1:n.*444C=
NM_001164695.1:c.*531C= NP_001158167.1:n.*531C=
NM_203395.2:c.*344C= NP_981932.1:n.*344C=
NM_001318495.1:c.*344C= NP_001305424.1:n.*344C=
NR_134655.1:n.1527C=
NM_001164694.2:c.*444C= NP_001158166.1:n.*444C=
NM_001164695.2:c.*531C= NP_001158167.1:n.*531C=
NM_001318495.2:c.*344C= NP_001305424.1:n.*344C=
NM_203395.3:c.*344C= MANE Select NP_981932.1:n.*344C=
NR_134655.2:n.1407C=