Canonical Allele Identifier: CA414841873

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868686C>T (hg19) ; chrY:g.19706800C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706800C>T , CM000686.2:g.19706800C>T	GRCh38
NC_000024.9:g.21868686C>T , CM000686.1:g.21868686C>T	GRCh37
NC_000024.8:g.20328074C>T	NCBI36
NG_032920.1:g.43140G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.4063G>A MANE Select	ENSP00000322408.4:p.Gly1355Ser
ENST00000317961.8:c.4063G>A	ENSP00000322408.4:p.Gly1355Ser
ENST00000382806.6:c.3892G>A	ENSP00000372256.2:p.Gly1298Ser
ENST00000440077.5:c.3940G>A	ENSP00000398543.1:p.Gly1314Ser
ENST00000469599.6:n.2661G>A
ENST00000492117.1:n.3955G>A
ENST00000541639.5:c.4156G>A	ENSP00000444293.1:p.Gly1386Ser
NM_001146705.1:c.4156G>A	NP_001140177.1:p.Gly1386Ser
NM_001146706.1:c.3892G>A	NP_001140178.1:p.Gly1298Ser
NM_004653.4:c.4063G>A	NP_004644.2:p.Gly1355Ser
XM_005262560.1:c.3928G>A	XP_005262617.1:p.Gly1310Ser
XM_005262561.1:c.3832G>A	XP_005262618.1:p.Gly1278Ser
XM_011531468.1:c.3985G>A	XP_011529770.1:p.Gly1329Ser
XR_244571.2:n.4351G>A
XR_430568.2:n.4685G>A
XM_005262560.3:c.3928G>A	XP_005262617.1:p.Gly1310Ser
XM_005262561.3:c.3832G>A	XP_005262618.1:p.Gly1278Ser
XM_011531468.3:c.3985G>A	XP_011529770.1:p.Gly1329Ser
XM_024452495.1:c.2053G>A	XP_024308263.1:p.Gly685Ser
XM_024452496.1:c.1819G>A	XP_024308264.1:p.Gly607Ser
XR_001756009.2:n.4801G>A
XR_001756010.2:n.4801G>A
XR_001756011.2:n.4666G>A
XR_001756012.2:n.4814G>A
XR_001756013.2:n.4132G>A
XR_002958832.1:n.4233G>A
XR_002958834.1:n.4457G>A
XR_002958835.1:n.4340G>A
XR_002958836.1:n.5023G>A
XR_002958837.1:n.4830G>A
XR_244571.4:n.4350G>A
XR_430568.4:n.4684G>A
NM_001146706.2:c.3892G>A	NP_001140178.1:p.Gly1298Ser
NM_004653.5:c.4063G>A MANE Select	NP_004644.2:p.Gly1355Ser
NM_001146705.2:c.4156G>A	NP_001140177.1:p.Gly1386Ser