Canonical Allele Identifier: CA2844471374

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19705733C>A , CM000686.2:g.19705733C>A	GRCh38
NC_000024.9:g.21867619C>A , CM000686.1:g.21867619C>A	GRCh37
NC_000024.8:g.20327007C>A	NCBI36
NG_032920.1:g.44207G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.*262G>T MANE Select	ENSP00000322408.4:n.*262G>T
ENST00000317961.8:c.*262G>T	ENSP00000322408.4:n.*262G>T
ENST00000382806.6:c.*262G>T	ENSP00000372256.2:n.*262G>T
ENST00000469599.6:n.3633G>T
ENST00000492117.1:n.4927G>T
ENST00000541639.5:c.*262G>T	ENSP00000444293.1:n.*262G>T
NM_001146705.1:c.*262G>T	NP_001140177.1:n.*262G>T
NM_001146706.1:c.*262G>T	NP_001140178.1:n.*262G>T
NM_004653.4:c.*262G>T	NP_004644.2:n.*262G>T
XM_005262560.1:c.*262G>T	XP_005262617.1:n.*262G>T
XM_005262561.1:c.*262G>T	XP_005262618.1:n.*262G>T
XM_011531468.1:c.*262G>T	XP_011529770.1:n.*262G>T
XR_430568.2:n.5657G>T
XM_005262560.3:c.*262G>T	XP_005262617.1:n.*262G>T
XM_005262561.3:c.*262G>T	XP_005262618.1:n.*262G>T
XM_011531468.3:c.*262G>T	XP_011529770.1:n.*262G>T
XM_024452495.1:c.*262G>T	XP_024308263.1:n.*262G>T
XM_024452496.1:c.*262G>T	XP_024308264.1:n.*262G>T
XR_001756009.2:n.5620G>T
XR_001756010.2:n.5588G>T
XR_001756011.2:n.5485G>T
XR_001756012.2:n.5633G>T
XR_001756013.2:n.4951G>T
XR_002958832.1:n.5205G>T
XR_002958834.1:n.5276G>T
XR_002958835.1:n.5159G>T
XR_002958836.1:n.5810G>T
XR_002958837.1:n.5617G>T
XR_244571.4:n.5137G>T
XR_430568.4:n.5656G>T
NM_001146706.2:c.*262G>T	NP_001140178.1:n.*262G>T
NM_004653.5:c.*262G>T MANE Select	NP_004644.2:n.*262G>T
NM_001146705.2:c.*262G>T	NP_001140177.1:n.*262G>T