Canonical Allele Identifier: CA1672406039
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398698T= , CM000668.2:g.150398698T= GRCh38
NC_000006.11:g.150719834T= , CM000668.1:g.150719834T= GRCh37
NC_000006.10:g.150761527T= NCBI36
NG_016007.1:g.34807T=
NG_016007.2:g.34807T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*461T= MANE Select ENSP00000343763.4:n.*461T=
ENST00000229447.9:c.*561T= ENSP00000229447.5:n.*561T=
ENST00000344419.7:c.*461T= ENSP00000343763.3:n.*461T=
NM_001164694.1:c.*561T= NP_001158166.1:n.*561T=
NM_001164695.1:c.*648T= NP_001158167.1:n.*648T=
NM_203395.2:c.*461T= NP_981932.1:n.*461T=
NM_001318495.1:c.*461T= NP_001305424.1:n.*461T=
NR_134655.1:n.1644T=
NM_001164694.2:c.*561T= NP_001158166.1:n.*561T=
NM_001164695.2:c.*648T= NP_001158167.1:n.*648T=
NM_001318495.2:c.*461T= NP_001305424.1:n.*461T=
NM_203395.3:c.*461T= MANE Select NP_981932.1:n.*461T=
NR_134655.2:n.1524T=