Canonical Allele Identifier: CA10575005

Gene: KDM5D

Linked Data

• dbSNP Id: rs746730690
• ExAC: Y:21897362 G / A
• gnomAD v2: Y-21897362-G-A
• gnomAD v3: Y-19735476-G-A
• gnomAD v4: Y-19735476-G-A
• MyVariant Identifiers: chrY:g.21897362G>A (hg19) ; chrY:g.19735476G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19735476G>A , CM000686.2:g.19735476G>A	GRCh38
NC_000024.9:g.21897362G>A , CM000686.1:g.21897362G>A	GRCh37
NC_000024.8:g.20356750G>A	NCBI36
NG_032920.1:g.14464C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.809C>T MANE Select	ENSP00000322408.4:p.Thr270Met
ENST00000317961.8:c.809C>T	ENSP00000322408.4:p.Thr270Met
ENST00000382806.6:c.638C>T	ENSP00000372256.2:p.Thr213Met
ENST00000440077.5:c.686C>T	ENSP00000398543.1:p.Thr229Met
ENST00000447300.1:c.674C>T	ENSP00000416377.1:p.Thr225Met
ENST00000541639.5:c.809C>T	ENSP00000444293.1:p.Thr270Met
NM_001146705.1:c.809C>T	NP_001140177.1:p.Thr270Met
NM_001146706.1:c.638C>T	NP_001140178.1:p.Thr213Met
NM_004653.4:c.809C>T	NP_004644.2:p.Thr270Met
XM_005262560.1:c.674C>T	XP_005262617.1:p.Thr225Met
XM_005262561.1:c.809C>T	XP_005262618.1:p.Thr270Met
XM_005262562.2:c.809C>T	XP_005262619.1:p.Thr270Met
XM_011531468.1:c.809C>T	XP_011529770.1:p.Thr270Met
XR_244571.2:n.1097C>T
XR_430568.2:n.1097C>T
XR_938609.1:n.1097C>T
XR_938610.1:n.1097C>T
XM_005262560.3:c.674C>T	XP_005262617.1:p.Thr225Met
XM_005262561.3:c.809C>T	XP_005262618.1:p.Thr270Met
XM_011531468.3:c.809C>T	XP_011529770.1:p.Thr270Met
XM_024452495.1:c.-1309C>T	XP_024308263.1:n.-1309C>T
XR_001756009.2:n.1096C>T
XR_001756010.2:n.1096C>T
XR_001756011.2:n.961C>T
XR_001756012.2:n.1096C>T
XR_001756013.2:n.1096C>T
XR_002958832.1:n.1096C>T
XR_002958833.1:n.1096C>T
XR_002958834.1:n.1096C>T
XR_002958835.1:n.1096C>T
XR_002958836.1:n.1096C>T
XR_002958837.1:n.1096C>T
XR_244571.4:n.1096C>T
XR_430568.4:n.1096C>T
NM_001146706.2:c.638C>T	NP_001140178.1:p.Thr213Met
NM_004653.5:c.809C>T MANE Select	NP_004644.2:p.Thr270Met
NM_001146705.2:c.809C>T	NP_001140177.1:p.Thr270Met