Canonical Allele Identifier: CA1672406041
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398699A= , CM000668.2:g.150398699A= GRCh38
NC_000006.11:g.150719835A= , CM000668.1:g.150719835A= GRCh37
NC_000006.10:g.150761528A= NCBI36
NG_016007.1:g.34808A=
NG_016007.2:g.34808A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*462A= MANE Select ENSP00000343763.4:n.*462A=
ENST00000229447.9:c.*562A= ENSP00000229447.5:n.*562A=
ENST00000344419.7:c.*462A= ENSP00000343763.3:n.*462A=
NM_001164694.1:c.*562A= NP_001158166.1:n.*562A=
NM_001164695.1:c.*649A= NP_001158167.1:n.*649A=
NM_203395.2:c.*462A= NP_981932.1:n.*462A=
NM_001318495.1:c.*462A= NP_001305424.1:n.*462A=
NR_134655.1:n.1645A=
NM_001164694.2:c.*562A= NP_001158166.1:n.*562A=
NM_001164695.2:c.*649A= NP_001158167.1:n.*649A=
NM_001318495.2:c.*462A= NP_001305424.1:n.*462A=
NM_203395.3:c.*462A= MANE Select NP_981932.1:n.*462A=
NR_134655.2:n.1525A=