Canonical Allele Identifier: CA2506861270

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19705859G>A , CM000686.2:g.19705859G>A	GRCh38
NC_000024.9:g.21867745G>A , CM000686.1:g.21867745G>A	GRCh37
NC_000024.8:g.20327133G>A	NCBI36
NG_032920.1:g.44081C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.*136C>T MANE Select	ENSP00000322408.4:n.*136C>T
ENST00000317961.8:c.*136C>T	ENSP00000322408.4:n.*136C>T
ENST00000382806.6:c.*136C>T	ENSP00000372256.2:n.*136C>T
ENST00000469599.6:n.3507C>T
ENST00000492117.1:n.4801C>T
ENST00000541639.5:c.*136C>T	ENSP00000444293.1:n.*136C>T
NM_001146705.1:c.*136C>T	NP_001140177.1:n.*136C>T
NM_001146706.1:c.*136C>T	NP_001140178.1:n.*136C>T
NM_004653.4:c.*136C>T	NP_004644.2:n.*136C>T
XM_005262560.1:c.*136C>T	XP_005262617.1:n.*136C>T
XM_005262561.1:c.*136C>T	XP_005262618.1:n.*136C>T
XM_011531468.1:c.*136C>T	XP_011529770.1:n.*136C>T
XR_430568.2:n.5531C>T
XM_005262560.3:c.*136C>T	XP_005262617.1:n.*136C>T
XM_005262561.3:c.*136C>T	XP_005262618.1:n.*136C>T
XM_011531468.3:c.*136C>T	XP_011529770.1:n.*136C>T
XM_024452495.1:c.*136C>T	XP_024308263.1:n.*136C>T
XM_024452496.1:c.*136C>T	XP_024308264.1:n.*136C>T
XR_001756009.2:n.5494C>T
XR_001756010.2:n.5462C>T
XR_001756011.2:n.5359C>T
XR_001756012.2:n.5507C>T
XR_001756013.2:n.4825C>T
XR_002958832.1:n.5079C>T
XR_002958834.1:n.5150C>T
XR_002958835.1:n.5033C>T
XR_002958836.1:n.5684C>T
XR_002958837.1:n.5491C>T
XR_244571.4:n.5011C>T
XR_430568.4:n.5530C>T
NM_001146706.2:c.*136C>T	NP_001140178.1:n.*136C>T
NM_004653.5:c.*136C>T MANE Select	NP_004644.2:n.*136C>T
NM_001146705.2:c.*136C>T	NP_001140177.1:n.*136C>T