Canonical Allele Identifier: CA1672406106
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398835A= , CM000668.2:g.150398835A= GRCh38
NC_000006.11:g.150719971A= , CM000668.1:g.150719971A= GRCh37
NC_000006.10:g.150761664A= NCBI36
NG_016007.1:g.34944A=
NG_016007.2:g.34944A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*598A= MANE Select ENSP00000343763.4:n.*598A=
ENST00000229447.9:c.*698A= ENSP00000229447.5:n.*698A=
ENST00000344419.7:c.*598A= ENSP00000343763.3:n.*598A=
NM_001164694.1:c.*698A= NP_001158166.1:n.*698A=
NM_001164695.1:c.*785A= NP_001158167.1:n.*785A=
NM_203395.2:c.*598A= NP_981932.1:n.*598A=
NM_001318495.1:c.*598A= NP_001305424.1:n.*598A=
NR_134655.1:n.1781A=
NM_001164694.2:c.*698A= NP_001158166.1:n.*698A=
NM_001164695.2:c.*785A= NP_001158167.1:n.*785A=
NM_001318495.2:c.*598A= NP_001305424.1:n.*598A=
NM_203395.3:c.*598A= MANE Select NP_981932.1:n.*598A=
NR_134655.2:n.1661A=