Canonical Allele Identifier: CA2470919006
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19708000C= , CM000686.2:g.19708000C= GRCh38
NC_000024.9:g.21869886C= , CM000686.1:g.21869886C= GRCh37
NC_000024.8:g.20329274C= NCBI36
NG_032920.1:g.41940G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3333G= MANE Select ENSP00000322408.4:p.Gly1111=
ENST00000317961.8:c.3333G= ENSP00000322408.4:p.Gly1111=
ENST00000382806.6:c.3162G= ENSP00000372256.2:p.Gly1054=
ENST00000415360.1:c.249G= ENSP00000389433.1:p.Gly83=
ENST00000440077.5:c.3210G= ENSP00000398543.1:p.Gly1070=
ENST00000469599.6:n.1931G=
ENST00000492117.1:n.3225G=
ENST00000541639.5:c.3426G= ENSP00000444293.1:p.Gly1142=
NM_001146705.1:c.3426G= NP_001140177.1:p.Gly1142=
NM_001146706.1:c.3162G= NP_001140178.1:p.Gly1054=
NM_004653.4:c.3333G= NP_004644.2:p.Gly1111=
XM_005262560.1:c.3198G= XP_005262617.1:p.Gly1066=
XM_005262561.1:c.3102G= XP_005262618.1:p.Gly1034=
XM_011531468.1:c.3255G= XP_011529770.1:p.Gly1085=
XR_244571.2:n.3621G=
XR_430568.2:n.3955G=
XM_005262560.3:c.3198G= XP_005262617.1:p.Gly1066=
XM_005262561.3:c.3102G= XP_005262618.1:p.Gly1034=
XM_011531468.3:c.3255G= XP_011529770.1:p.Gly1085=
XM_024452495.1:c.1323G= XP_024308263.1:p.Gly441=
XM_024452496.1:c.1089G= XP_024308264.1:p.Gly363=
XR_001756009.2:n.4071G=
XR_001756010.2:n.4071G=
XR_001756011.2:n.3936G=
XR_001756012.2:n.4084G=
XR_001756013.2:n.3402G=
XR_002958832.1:n.3503G=
XR_002958834.1:n.3727G=
XR_002958835.1:n.3610G=
XR_002958836.1:n.4293G=
XR_002958837.1:n.4100G=
XR_244571.4:n.3620G=
XR_430568.4:n.3954G=
NM_001146706.2:c.3162G= NP_001140178.1:p.Gly1054=
NM_004653.5:c.3333G= MANE Select NP_004644.2:p.Gly1111=
NM_001146705.2:c.3426G= NP_001140177.1:p.Gly1142=