Canonical Allele Identifier: CA520159974

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868705C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706819C>T , CM000686.2:g.19706819C>T	GRCh38
NC_000024.9:g.21868705C>T , CM000686.1:g.21868705C>T	GRCh37
NC_000024.8:g.20328093C>T	NCBI36
NG_032920.1:g.43121G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4044G>A MANE Select	ENSP00000322408.4:p.Glu1348=
ENST00000317961.8:c.4044G>A	ENSP00000322408.4:p.Glu1348=
ENST00000382806.6:c.3873G>A	ENSP00000372256.2:p.Glu1291=
ENST00000440077.5:c.3921G>A	ENSP00000398543.1:p.Glu1307=
ENST00000469599.6:n.2642G>A
ENST00000492117.1:n.3936G>A
ENST00000541639.5:c.4137G>A	ENSP00000444293.1:p.Glu1379=
NM_001146705.1:c.4137G>A	NP_001140177.1:p.Glu1379=
NM_001146706.1:c.3873G>A	NP_001140178.1:p.Glu1291=
NM_004653.4:c.4044G>A	NP_004644.2:p.Glu1348=
XM_005262560.1:c.3909G>A	XP_005262617.1:p.Glu1303=
XM_005262561.1:c.3813G>A	XP_005262618.1:p.Glu1271=
XM_011531468.1:c.3966G>A	XP_011529770.1:p.Glu1322=
XR_244571.2:n.4332G>A
XR_430568.2:n.4666G>A
XM_005262560.3:c.3909G>A	XP_005262617.1:p.Glu1303=
XM_005262561.3:c.3813G>A	XP_005262618.1:p.Glu1271=
XM_011531468.3:c.3966G>A	XP_011529770.1:p.Glu1322=
XM_024452495.1:c.2034G>A	XP_024308263.1:p.Glu678=
XM_024452496.1:c.1800G>A	XP_024308264.1:p.Glu600=
XR_001756009.2:n.4782G>A
XR_001756010.2:n.4782G>A
XR_001756011.2:n.4647G>A
XR_001756012.2:n.4795G>A
XR_001756013.2:n.4113G>A
XR_002958832.1:n.4214G>A
XR_002958834.1:n.4438G>A
XR_002958835.1:n.4321G>A
XR_002958836.1:n.5004G>A
XR_002958837.1:n.4811G>A
XR_244571.4:n.4331G>A
XR_430568.4:n.4665G>A
NM_001146706.2:c.3873G>A	NP_001140178.1:p.Glu1291=
NM_004653.5:c.4044G>A MANE Select	NP_004644.2:p.Glu1348=
NM_001146705.2:c.4137G>A	NP_001140177.1:p.Glu1379=