Canonical Allele Identifier: CA520159464

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21867995A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706109A>C , CM000686.2:g.19706109A>C	GRCh38
NC_000024.9:g.21867995A>C , CM000686.1:g.21867995A>C	GRCh37
NC_000024.8:g.20327383A>C	NCBI36
NG_032920.1:g.43831T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4506T>G MANE Select	ENSP00000322408.4:p.Pro1502=
ENST00000317961.8:c.4506T>G	ENSP00000322408.4:p.Pro1502=
ENST00000382806.6:c.4335T>G	ENSP00000372256.2:p.Pro1445=
ENST00000440077.5:c.4383T>G	ENSP00000398543.1:p.Pro1461=
ENST00000469599.6:n.3257T>G
ENST00000492117.1:n.4551T>G
ENST00000541639.5:c.4599T>G	ENSP00000444293.1:p.Pro1533=
NM_001146705.1:c.4599T>G	NP_001140177.1:p.Pro1533=
NM_001146706.1:c.4335T>G	NP_001140178.1:p.Pro1445=
NM_004653.4:c.4506T>G	NP_004644.2:p.Pro1502=
XM_005262560.1:c.4371T>G	XP_005262617.1:p.Pro1457=
XM_005262561.1:c.4275T>G	XP_005262618.1:p.Pro1425=
XM_011531468.1:c.4428T>G	XP_011529770.1:p.Pro1476=
XR_430568.2:n.5281T>G
XM_005262560.3:c.4371T>G	XP_005262617.1:p.Pro1457=
XM_005262561.3:c.4275T>G	XP_005262618.1:p.Pro1425=
XM_011531468.3:c.4428T>G	XP_011529770.1:p.Pro1476=
XM_024452495.1:c.2496T>G	XP_024308263.1:p.Pro832=
XM_024452496.1:c.2262T>G	XP_024308264.1:p.Pro754=
XR_001756009.2:n.5244T>G
XR_001756010.2:n.5212T>G
XR_001756011.2:n.5109T>G
XR_001756012.2:n.5257T>G
XR_001756013.2:n.4575T>G
XR_002958832.1:n.4829T>G
XR_002958834.1:n.4900T>G
XR_002958835.1:n.4783T>G
XR_002958836.1:n.5434T>G
XR_002958837.1:n.5241T>G
XR_244571.4:n.4761T>G
XR_430568.4:n.5280T>G
NM_001146706.2:c.4335T>G	NP_001140178.1:p.Pro1445=
NM_004653.5:c.4506T>G MANE Select	NP_004644.2:p.Pro1502=
NM_001146705.2:c.4599T>G	NP_001140177.1:p.Pro1533=