Canonical Allele Identifier: CA2470918889
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19706910G= , CM000686.2:g.19706910G= GRCh38
NC_000024.9:g.21868796G= , CM000686.1:g.21868796G= GRCh37
NC_000024.8:g.20328184G= NCBI36
NG_032920.1:g.43030C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.4000-47C= MANE Select ENSP00000322408.4:n.4000-47C=
ENST00000317961.8:c.4000-47C= ENSP00000322408.4:n.4000-47C=
ENST00000382806.6:c.3829-47C= ENSP00000372256.2:n.3829-47C=
ENST00000440077.5:c.3877-47C= ENSP00000398543.1:n.3877-47C=
ENST00000469599.6:n.2598-47C=
ENST00000492117.1:n.3892-47C=
ENST00000541639.5:c.4093-47C= ENSP00000444293.1:n.4093-47C=
NM_001146705.1:c.4093-47C= NP_001140177.1:n.4093-47C=
NM_001146706.1:c.3829-47C= NP_001140178.1:n.3829-47C=
NM_004653.4:c.4000-47C= NP_004644.2:n.4000-47C=
XM_005262560.1:c.3865-47C= XP_005262617.1:n.3865-47C=
XM_005262561.1:c.3769-47C= XP_005262618.1:n.3769-47C=
XM_011531468.1:c.3922-47C= XP_011529770.1:n.3922-47C=
XR_244571.2:n.4288-47C=
XR_430568.2:n.4622-47C=
XM_005262560.3:c.3865-47C= XP_005262617.1:n.3865-47C=
XM_005262561.3:c.3769-47C= XP_005262618.1:n.3769-47C=
XM_011531468.3:c.3922-47C= XP_011529770.1:n.3922-47C=
XM_024452495.1:c.1990-47C= XP_024308263.1:n.1990-47C=
XM_024452496.1:c.1756-47C= XP_024308264.1:n.1756-47C=
XR_001756009.2:n.4738-47C=
XR_001756010.2:n.4738-47C=
XR_001756011.2:n.4603-47C=
XR_001756012.2:n.4751-47C=
XR_001756013.2:n.4069-47C=
XR_002958832.1:n.4170-47C=
XR_002958834.1:n.4394-47C=
XR_002958835.1:n.4277-47C=
XR_002958836.1:n.4960-47C=
XR_002958837.1:n.4767-47C=
XR_244571.4:n.4287-47C=
XR_430568.4:n.4621-47C=
NM_001146706.2:c.3829-47C= NP_001140178.1:n.3829-47C=
NM_004653.5:c.4000-47C= MANE Select NP_004644.2:n.4000-47C=
NM_001146705.2:c.4093-47C= NP_001140177.1:n.4093-47C=