Canonical Allele Identifier: CA520159496

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868007T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706121T>A , CM000686.2:g.19706121T>A	GRCh38
NC_000024.9:g.21868007T>A , CM000686.1:g.21868007T>A	GRCh37
NC_000024.8:g.20327395T>A	NCBI36
NG_032920.1:g.43819A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4494A>T MANE Select	ENSP00000322408.4:p.Thr1498=
ENST00000317961.8:c.4494A>T	ENSP00000322408.4:p.Thr1498=
ENST00000382806.6:c.4323A>T	ENSP00000372256.2:p.Thr1441=
ENST00000440077.5:c.4371A>T	ENSP00000398543.1:p.Thr1457=
ENST00000469599.6:n.3245A>T
ENST00000492117.1:n.4539A>T
ENST00000541639.5:c.4587A>T	ENSP00000444293.1:p.Thr1529=
NM_001146705.1:c.4587A>T	NP_001140177.1:p.Thr1529=
NM_001146706.1:c.4323A>T	NP_001140178.1:p.Thr1441=
NM_004653.4:c.4494A>T	NP_004644.2:p.Thr1498=
XM_005262560.1:c.4359A>T	XP_005262617.1:p.Thr1453=
XM_005262561.1:c.4263A>T	XP_005262618.1:p.Thr1421=
XM_011531468.1:c.4416A>T	XP_011529770.1:p.Thr1472=
XR_430568.2:n.5269A>T
XM_005262560.3:c.4359A>T	XP_005262617.1:p.Thr1453=
XM_005262561.3:c.4263A>T	XP_005262618.1:p.Thr1421=
XM_011531468.3:c.4416A>T	XP_011529770.1:p.Thr1472=
XM_024452495.1:c.2484A>T	XP_024308263.1:p.Thr828=
XM_024452496.1:c.2250A>T	XP_024308264.1:p.Thr750=
XR_001756009.2:n.5232A>T
XR_001756010.2:n.5200A>T
XR_001756011.2:n.5097A>T
XR_001756012.2:n.5245A>T
XR_001756013.2:n.4563A>T
XR_002958832.1:n.4817A>T
XR_002958834.1:n.4888A>T
XR_002958835.1:n.4771A>T
XR_002958836.1:n.5422A>T
XR_002958837.1:n.5229A>T
XR_244571.4:n.4749A>T
XR_430568.4:n.5268A>T
NM_001146706.2:c.4323A>T	NP_001140178.1:p.Thr1441=
NM_004653.5:c.4494A>T MANE Select	NP_004644.2:p.Thr1498=
NM_001146705.2:c.4587A>T	NP_001140177.1:p.Thr1529=