Canonical Allele Identifier: CA414840226

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868009T>C (hg19) ; chrY:g.19706123T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706123T>C , CM000686.2:g.19706123T>C	GRCh38
NC_000024.9:g.21868009T>C , CM000686.1:g.21868009T>C	GRCh37
NC_000024.8:g.20327397T>C	NCBI36
NG_032920.1:g.43817A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4492A>G MANE Select	ENSP00000322408.4:p.Thr1498Ala
ENST00000317961.8:c.4492A>G	ENSP00000322408.4:p.Thr1498Ala
ENST00000382806.6:c.4321A>G	ENSP00000372256.2:p.Thr1441Ala
ENST00000440077.5:c.4369A>G	ENSP00000398543.1:p.Thr1457Ala
ENST00000469599.6:n.3243A>G
ENST00000492117.1:n.4537A>G
ENST00000541639.5:c.4585A>G	ENSP00000444293.1:p.Thr1529Ala
NM_001146705.1:c.4585A>G	NP_001140177.1:p.Thr1529Ala
NM_001146706.1:c.4321A>G	NP_001140178.1:p.Thr1441Ala
NM_004653.4:c.4492A>G	NP_004644.2:p.Thr1498Ala
XM_005262560.1:c.4357A>G	XP_005262617.1:p.Thr1453Ala
XM_005262561.1:c.4261A>G	XP_005262618.1:p.Thr1421Ala
XM_011531468.1:c.4414A>G	XP_011529770.1:p.Thr1472Ala
XR_430568.2:n.5267A>G
XM_005262560.3:c.4357A>G	XP_005262617.1:p.Thr1453Ala
XM_005262561.3:c.4261A>G	XP_005262618.1:p.Thr1421Ala
XM_011531468.3:c.4414A>G	XP_011529770.1:p.Thr1472Ala
XM_024452495.1:c.2482A>G	XP_024308263.1:p.Thr828Ala
XM_024452496.1:c.2248A>G	XP_024308264.1:p.Thr750Ala
XR_001756009.2:n.5230A>G
XR_001756010.2:n.5198A>G
XR_001756011.2:n.5095A>G
XR_001756012.2:n.5243A>G
XR_001756013.2:n.4561A>G
XR_002958832.1:n.4815A>G
XR_002958834.1:n.4886A>G
XR_002958835.1:n.4769A>G
XR_002958836.1:n.5420A>G
XR_002958837.1:n.5227A>G
XR_244571.4:n.4747A>G
XR_430568.4:n.5266A>G
NM_001146706.2:c.4321A>G	NP_001140178.1:p.Thr1441Ala
NM_004653.5:c.4492A>G MANE Select	NP_004644.2:p.Thr1498Ala
NM_001146705.2:c.4585A>G	NP_001140177.1:p.Thr1529Ala