Canonical Allele Identifier: CA2470920630
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19732043T= , CM000686.2:g.19732043T= GRCh38
NC_000024.9:g.21893929T= , CM000686.1:g.21893929T= GRCh37
NC_000024.8:g.20353317T= NCBI36
NG_032920.1:g.17897A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.1212+3A= MANE Select ENSP00000322408.4:n.1212+3A=
ENST00000317961.8:c.1212+3A= ENSP00000322408.4:n.1212+3A=
ENST00000382806.6:c.1041+3A= ENSP00000372256.2:n.1041+3A=
ENST00000440077.5:c.1089+3A= ENSP00000398543.1:n.1089+3A=
ENST00000447300.1:c.1077+3A= ENSP00000416377.1:n.1077+3A=
ENST00000541639.5:c.1212+3A= ENSP00000444293.1:n.1212+3A=
NM_001146705.1:c.1212+3A= NP_001140177.1:n.1212+3A=
NM_001146706.1:c.1041+3A= NP_001140178.1:n.1041+3A=
NM_004653.4:c.1212+3A= NP_004644.2:n.1212+3A=
XM_005262560.1:c.1077+3A= XP_005262617.1:n.1077+3A=
XM_005262561.1:c.1212+3A= XP_005262618.1:n.1212+3A=
XM_005262562.2:c.1212+3A= XP_005262619.1:n.1212+3A=
XM_011531468.1:c.1212+3A= XP_011529770.1:n.1212+3A=
XR_244571.2:n.1500+3A=
XR_430568.2:n.1500+3A=
XR_938609.1:n.1500+3A=
XR_938610.1:n.1500+3A=
XM_005262560.3:c.1077+3A= XP_005262617.1:n.1077+3A=
XM_005262561.3:c.1212+3A= XP_005262618.1:n.1212+3A=
XM_011531468.3:c.1212+3A= XP_011529770.1:n.1212+3A=
XM_024452495.1:c.-906+3A= XP_024308263.1:n.-906+3A=
XR_001756009.2:n.1499+3A=
XR_001756010.2:n.1499+3A=
XR_001756011.2:n.1364+3A=
XR_001756012.2:n.1499+3A=
XR_001756013.2:n.1499+3A=
XR_002958832.1:n.1499+3A=
XR_002958833.1:n.1499+3A=
XR_002958834.1:n.1499+3A=
XR_002958835.1:n.1499+3A=
XR_002958836.1:n.1499+3A=
XR_002958837.1:n.1499+3A=
XR_244571.4:n.1499+3A=
XR_430568.4:n.1499+3A=
NM_001146706.2:c.1041+3A= NP_001140178.1:n.1041+3A=
NM_004653.5:c.1212+3A= MANE Select NP_004644.2:n.1212+3A=
NM_001146705.2:c.1212+3A= NP_001140177.1:n.1212+3A=