Canonical Allele Identifier: CA2470919018
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19708060C= , CM000686.2:g.19708060C= GRCh38
NC_000024.9:g.21869946C= , CM000686.1:g.21869946C= GRCh37
NC_000024.8:g.20329334C= NCBI36
NG_032920.1:g.41880G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3273G= MANE Select ENSP00000322408.4:p.Pro1091=
ENST00000317961.8:c.3273G= ENSP00000322408.4:p.Pro1091=
ENST00000382806.6:c.3102G= ENSP00000372256.2:p.Pro1034=
ENST00000415360.1:c.189G= ENSP00000389433.1:p.Pro63=
ENST00000440077.5:c.3150G= ENSP00000398543.1:p.Pro1050=
ENST00000469599.6:n.1871G=
ENST00000492117.1:n.3165G=
ENST00000541639.5:c.3366G= ENSP00000444293.1:p.Pro1122=
NM_001146705.1:c.3366G= NP_001140177.1:p.Pro1122=
NM_001146706.1:c.3102G= NP_001140178.1:p.Pro1034=
NM_004653.4:c.3273G= NP_004644.2:p.Pro1091=
XM_005262560.1:c.3138G= XP_005262617.1:p.Pro1046=
XM_005262561.1:c.3042G= XP_005262618.1:p.Pro1014=
XM_011531468.1:c.3195G= XP_011529770.1:p.Pro1065=
XR_244571.2:n.3561G=
XR_430568.2:n.3895G=
XM_005262560.3:c.3138G= XP_005262617.1:p.Pro1046=
XM_005262561.3:c.3042G= XP_005262618.1:p.Pro1014=
XM_011531468.3:c.3195G= XP_011529770.1:p.Pro1065=
XM_024452495.1:c.1263G= XP_024308263.1:p.Pro421=
XM_024452496.1:c.1029G= XP_024308264.1:p.Pro343=
XR_001756009.2:n.4011G=
XR_001756010.2:n.4011G=
XR_001756011.2:n.3876G=
XR_001756012.2:n.4024G=
XR_001756013.2:n.3342G=
XR_002958832.1:n.3443G=
XR_002958834.1:n.3667G=
XR_002958835.1:n.3550G=
XR_002958836.1:n.4233G=
XR_002958837.1:n.4040G=
XR_244571.4:n.3560G=
XR_430568.4:n.3894G=
NM_001146706.2:c.3102G= NP_001140178.1:p.Pro1034=
NM_004653.5:c.3273G= MANE Select NP_004644.2:p.Pro1091=
NM_001146705.2:c.3366G= NP_001140177.1:p.Pro1122=