Canonical Allele Identifier: CA2766253074

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19705678T>A , CM000686.2:g.19705678T>A	GRCh38
NC_000024.9:g.21867564T>A , CM000686.1:g.21867564T>A	GRCh37
NC_000024.8:g.20326952T>A	NCBI36
NG_032920.1:g.44262A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.*317A>T MANE Select	ENSP00000322408.4:n.*317A>T
ENST00000317961.8:c.*317A>T	ENSP00000322408.4:n.*317A>T
ENST00000382806.6:c.*317A>T	ENSP00000372256.2:n.*317A>T
ENST00000469599.6:n.3688A>T
ENST00000492117.1:n.4982A>T
ENST00000541639.5:c.*317A>T	ENSP00000444293.1:n.*317A>T
NM_001146705.1:c.*317A>T	NP_001140177.1:n.*317A>T
NM_001146706.1:c.*317A>T	NP_001140178.1:n.*317A>T
NM_004653.4:c.*317A>T	NP_004644.2:n.*317A>T
XM_005262560.1:c.*317A>T	XP_005262617.1:n.*317A>T
XM_005262561.1:c.*317A>T	XP_005262618.1:n.*317A>T
XM_011531468.1:c.*317A>T	XP_011529770.1:n.*317A>T
XR_430568.2:n.5712A>T
XM_005262560.3:c.*317A>T	XP_005262617.1:n.*317A>T
XM_005262561.3:c.*317A>T	XP_005262618.1:n.*317A>T
XM_011531468.3:c.*317A>T	XP_011529770.1:n.*317A>T
XM_024452495.1:c.*317A>T	XP_024308263.1:n.*317A>T
XM_024452496.1:c.*317A>T	XP_024308264.1:n.*317A>T
XR_001756009.2:n.5675A>T
XR_001756010.2:n.5643A>T
XR_001756011.2:n.5540A>T
XR_001756012.2:n.5688A>T
XR_001756013.2:n.5006A>T
XR_002958832.1:n.5260A>T
XR_002958834.1:n.5331A>T
XR_002958835.1:n.5214A>T
XR_002958836.1:n.5865A>T
XR_002958837.1:n.5672A>T
XR_244571.4:n.5192A>T
XR_430568.4:n.5711A>T
NM_001146706.2:c.*317A>T	NP_001140178.1:n.*317A>T
NM_004653.5:c.*317A>T MANE Select	NP_004644.2:n.*317A>T
NM_001146705.2:c.*317A>T	NP_001140177.1:n.*317A>T