Canonical Allele Identifier: CA2470918953
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707456C= , CM000686.2:g.19707456C= GRCh38
NC_000024.9:g.21869342C= , CM000686.1:g.21869342C= GRCh37
NC_000024.8:g.20328730C= NCBI36
NG_032920.1:g.42484G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3690G= MANE Select ENSP00000322408.4:p.Leu1230=
ENST00000317961.8:c.3690G= ENSP00000322408.4:p.Leu1230=
ENST00000382806.6:c.3519G= ENSP00000372256.2:p.Leu1173=
ENST00000415360.1:c.606G= ENSP00000389433.1:p.Leu202=
ENST00000440077.5:c.3567G= ENSP00000398543.1:p.Leu1189=
ENST00000469599.6:n.2288G=
ENST00000492117.1:n.3582G=
ENST00000541639.5:c.3783G= ENSP00000444293.1:p.Leu1261=
NM_001146705.1:c.3783G= NP_001140177.1:p.Leu1261=
NM_001146706.1:c.3519G= NP_001140178.1:p.Leu1173=
NM_004653.4:c.3690G= NP_004644.2:p.Leu1230=
XM_005262560.1:c.3555G= XP_005262617.1:p.Leu1185=
XM_005262561.1:c.3459G= XP_005262618.1:p.Leu1153=
XM_011531468.1:c.3612G= XP_011529770.1:p.Leu1204=
XR_244571.2:n.3978G=
XR_430568.2:n.4312G=
XM_005262560.3:c.3555G= XP_005262617.1:p.Leu1185=
XM_005262561.3:c.3459G= XP_005262618.1:p.Leu1153=
XM_011531468.3:c.3612G= XP_011529770.1:p.Leu1204=
XM_024452495.1:c.1680G= XP_024308263.1:p.Leu560=
XM_024452496.1:c.1446G= XP_024308264.1:p.Leu482=
XR_001756009.2:n.4428G=
XR_001756010.2:n.4428G=
XR_001756011.2:n.4293G=
XR_001756012.2:n.4441G=
XR_001756013.2:n.3759G=
XR_002958832.1:n.3860G=
XR_002958834.1:n.4084G=
XR_002958835.1:n.3967G=
XR_002958836.1:n.4650G=
XR_002958837.1:n.4457G=
XR_244571.4:n.3977G=
XR_430568.4:n.4311G=
NM_001146706.2:c.3519G= NP_001140178.1:p.Leu1173=
NM_004653.5:c.3690G= MANE Select NP_004644.2:p.Leu1230=
NM_001146705.2:c.3783G= NP_001140177.1:p.Leu1261=