Canonical Allele Identifier: CA2470918952
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707450T= , CM000686.2:g.19707450T= GRCh38
NC_000024.9:g.21869336T= , CM000686.1:g.21869336T= GRCh37
NC_000024.8:g.20328724T= NCBI36
NG_032920.1:g.42490A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3696A= MANE Select ENSP00000322408.4:p.Pro1232=
ENST00000317961.8:c.3696A= ENSP00000322408.4:p.Pro1232=
ENST00000382806.6:c.3525A= ENSP00000372256.2:p.Pro1175=
ENST00000415360.1:c.612A= ENSP00000389433.1:p.Pro204=
ENST00000440077.5:c.3573A= ENSP00000398543.1:p.Pro1191=
ENST00000469599.6:n.2294A=
ENST00000492117.1:n.3588A=
ENST00000541639.5:c.3789A= ENSP00000444293.1:p.Pro1263=
NM_001146705.1:c.3789A= NP_001140177.1:p.Pro1263=
NM_001146706.1:c.3525A= NP_001140178.1:p.Pro1175=
NM_004653.4:c.3696A= NP_004644.2:p.Pro1232=
XM_005262560.1:c.3561A= XP_005262617.1:p.Pro1187=
XM_005262561.1:c.3465A= XP_005262618.1:p.Pro1155=
XM_011531468.1:c.3618A= XP_011529770.1:p.Pro1206=
XR_244571.2:n.3984A=
XR_430568.2:n.4318A=
XM_005262560.3:c.3561A= XP_005262617.1:p.Pro1187=
XM_005262561.3:c.3465A= XP_005262618.1:p.Pro1155=
XM_011531468.3:c.3618A= XP_011529770.1:p.Pro1206=
XM_024452495.1:c.1686A= XP_024308263.1:p.Pro562=
XM_024452496.1:c.1452A= XP_024308264.1:p.Pro484=
XR_001756009.2:n.4434A=
XR_001756010.2:n.4434A=
XR_001756011.2:n.4299A=
XR_001756012.2:n.4447A=
XR_001756013.2:n.3765A=
XR_002958832.1:n.3866A=
XR_002958834.1:n.4090A=
XR_002958835.1:n.3973A=
XR_002958836.1:n.4656A=
XR_002958837.1:n.4463A=
XR_244571.4:n.3983A=
XR_430568.4:n.4317A=
NM_001146706.2:c.3525A= NP_001140178.1:p.Pro1175=
NM_004653.5:c.3696A= MANE Select NP_004644.2:p.Pro1232=
NM_001146705.2:c.3789A= NP_001140177.1:p.Pro1263=