Canonical Allele Identifier: CA2470920844
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19735405G= , CM000686.2:g.19735405G= GRCh38
NC_000024.9:g.21897291G= , CM000686.1:g.21897291G= GRCh37
NC_000024.8:g.20356679G= NCBI36
NG_032920.1:g.14535C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.880C= MANE Select ENSP00000322408.4:p.Pro294=
ENST00000317961.8:c.880C= ENSP00000322408.4:p.Pro294=
ENST00000382806.6:c.709C= ENSP00000372256.2:p.Pro237=
ENST00000440077.5:c.757C= ENSP00000398543.1:p.Pro253=
ENST00000447300.1:c.745C= ENSP00000416377.1:p.Pro249=
ENST00000541639.5:c.880C= ENSP00000444293.1:p.Pro294=
NM_001146705.1:c.880C= NP_001140177.1:p.Pro294=
NM_001146706.1:c.709C= NP_001140178.1:p.Pro237=
NM_004653.4:c.880C= NP_004644.2:p.Pro294=
XM_005262560.1:c.745C= XP_005262617.1:p.Pro249=
XM_005262561.1:c.880C= XP_005262618.1:p.Pro294=
XM_005262562.2:c.880C= XP_005262619.1:p.Pro294=
XM_011531468.1:c.880C= XP_011529770.1:p.Pro294=
XR_244571.2:n.1168C=
XR_430568.2:n.1168C=
XR_938609.1:n.1168C=
XR_938610.1:n.1168C=
XM_005262560.3:c.745C= XP_005262617.1:p.Pro249=
XM_005262561.3:c.880C= XP_005262618.1:p.Pro294=
XM_011531468.3:c.880C= XP_011529770.1:p.Pro294=
XM_024452495.1:c.-1238C= XP_024308263.1:n.-1238C=
XR_001756009.2:n.1167C=
XR_001756010.2:n.1167C=
XR_001756011.2:n.1032C=
XR_001756012.2:n.1167C=
XR_001756013.2:n.1167C=
XR_002958832.1:n.1167C=
XR_002958833.1:n.1167C=
XR_002958834.1:n.1167C=
XR_002958835.1:n.1167C=
XR_002958836.1:n.1167C=
XR_002958837.1:n.1167C=
XR_244571.4:n.1167C=
XR_430568.4:n.1167C=
NM_001146706.2:c.709C= NP_001140178.1:p.Pro237=
NM_004653.5:c.880C= MANE Select NP_004644.2:p.Pro294=
NM_001146705.2:c.880C= NP_001140177.1:p.Pro294=