Canonical Allele Identifier: CA2840065419

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19732545C>A , CM000686.2:g.19732545C>A	GRCh38
NC_000024.9:g.21894431C>A , CM000686.1:g.21894431C>A	GRCh37
NC_000024.8:g.20353819C>A	NCBI36
NG_032920.1:g.17395G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.1092+39G>T MANE Select	ENSP00000322408.4:n.1092+39G>T
ENST00000317961.8:c.1092+39G>T	ENSP00000322408.4:n.1092+39G>T
ENST00000382806.6:c.921+39G>T	ENSP00000372256.2:n.921+39G>T
ENST00000440077.5:c.969+39G>T	ENSP00000398543.1:n.969+39G>T
ENST00000447300.1:c.957+39G>T	ENSP00000416377.1:n.957+39G>T
ENST00000541639.5:c.1092+39G>T	ENSP00000444293.1:n.1092+39G>T
NM_001146705.1:c.1092+39G>T	NP_001140177.1:n.1092+39G>T
NM_001146706.1:c.921+39G>T	NP_001140178.1:n.921+39G>T
NM_004653.4:c.1092+39G>T	NP_004644.2:n.1092+39G>T
XM_005262560.1:c.957+39G>T	XP_005262617.1:n.957+39G>T
XM_005262561.1:c.1092+39G>T	XP_005262618.1:n.1092+39G>T
XM_005262562.2:c.1092+39G>T	XP_005262619.1:n.1092+39G>T
XM_011531468.1:c.1092+39G>T	XP_011529770.1:n.1092+39G>T
XR_244571.2:n.1380+39G>T
XR_430568.2:n.1380+39G>T
XR_938609.1:n.1380+39G>T
XR_938610.1:n.1380+39G>T
XM_005262560.3:c.957+39G>T	XP_005262617.1:n.957+39G>T
XM_005262561.3:c.1092+39G>T	XP_005262618.1:n.1092+39G>T
XM_011531468.3:c.1092+39G>T	XP_011529770.1:n.1092+39G>T
XM_024452495.1:c.-1026+39G>T	XP_024308263.1:n.-1026+39G>T
XR_001756009.2:n.1379+39G>T
XR_001756010.2:n.1379+39G>T
XR_001756011.2:n.1244+39G>T
XR_001756012.2:n.1379+39G>T
XR_001756013.2:n.1379+39G>T
XR_002958832.1:n.1379+39G>T
XR_002958833.1:n.1379+39G>T
XR_002958834.1:n.1379+39G>T
XR_002958835.1:n.1379+39G>T
XR_002958836.1:n.1379+39G>T
XR_002958837.1:n.1379+39G>T
XR_244571.4:n.1379+39G>T
XR_430568.4:n.1379+39G>T
NM_001146706.2:c.921+39G>T	NP_001140178.1:n.921+39G>T
NM_004653.5:c.1092+39G>T MANE Select	NP_004644.2:n.1092+39G>T
NM_001146705.2:c.1092+39G>T	NP_001140177.1:n.1092+39G>T