Canonical Allele Identifier: CA414842838

Gene: KDM5D

Linked Data

• dbSNP Id: rs2045501152
• MyVariant Identifiers: chrY:g.21897320G>C (hg19) ; chrY:g.19735434G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19735434G>C , CM000686.2:g.19735434G>C	GRCh38
NC_000024.9:g.21897320G>C , CM000686.1:g.21897320G>C	GRCh37
NC_000024.8:g.20356708G>C	NCBI36
NG_032920.1:g.14506C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.851C>G MANE Select	ENSP00000322408.4:p.Thr284Arg
ENST00000317961.8:c.851C>G	ENSP00000322408.4:p.Thr284Arg
ENST00000382806.6:c.680C>G	ENSP00000372256.2:p.Thr227Arg
ENST00000440077.5:c.728C>G	ENSP00000398543.1:p.Thr243Arg
ENST00000447300.1:c.716C>G	ENSP00000416377.1:p.Thr239Arg
ENST00000541639.5:c.851C>G	ENSP00000444293.1:p.Thr284Arg
NM_001146705.1:c.851C>G	NP_001140177.1:p.Thr284Arg
NM_001146706.1:c.680C>G	NP_001140178.1:p.Thr227Arg
NM_004653.4:c.851C>G	NP_004644.2:p.Thr284Arg
XM_005262560.1:c.716C>G	XP_005262617.1:p.Thr239Arg
XM_005262561.1:c.851C>G	XP_005262618.1:p.Thr284Arg
XM_005262562.2:c.851C>G	XP_005262619.1:p.Thr284Arg
XM_011531468.1:c.851C>G	XP_011529770.1:p.Thr284Arg
XR_244571.2:n.1139C>G
XR_430568.2:n.1139C>G
XR_938609.1:n.1139C>G
XR_938610.1:n.1139C>G
XM_005262560.3:c.716C>G	XP_005262617.1:p.Thr239Arg
XM_005262561.3:c.851C>G	XP_005262618.1:p.Thr284Arg
XM_011531468.3:c.851C>G	XP_011529770.1:p.Thr284Arg
XM_024452495.1:c.-1267C>G	XP_024308263.1:n.-1267C>G
XR_001756009.2:n.1138C>G
XR_001756010.2:n.1138C>G
XR_001756011.2:n.1003C>G
XR_001756012.2:n.1138C>G
XR_001756013.2:n.1138C>G
XR_002958832.1:n.1138C>G
XR_002958833.1:n.1138C>G
XR_002958834.1:n.1138C>G
XR_002958835.1:n.1138C>G
XR_002958836.1:n.1138C>G
XR_002958837.1:n.1138C>G
XR_244571.4:n.1138C>G
XR_430568.4:n.1138C>G
NM_001146706.2:c.680C>G	NP_001140178.1:p.Thr227Arg
NM_004653.5:c.851C>G MANE Select	NP_004644.2:p.Thr284Arg
NM_001146705.2:c.851C>G	NP_001140177.1:p.Thr284Arg