Canonical Allele Identifier: CA520514668

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868016T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706130T>C , CM000686.2:g.19706130T>C	GRCh38
NC_000024.9:g.21868016T>C , CM000686.1:g.21868016T>C	GRCh37
NC_000024.8:g.20327404T>C	NCBI36
NG_032920.1:g.43810A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4485A>G MANE Select	ENSP00000322408.4:p.Thr1495=
ENST00000317961.8:c.4485A>G	ENSP00000322408.4:p.Thr1495=
ENST00000382806.6:c.4314A>G	ENSP00000372256.2:p.Thr1438=
ENST00000440077.5:c.4362A>G	ENSP00000398543.1:p.Thr1454=
ENST00000469599.6:n.3236A>G
ENST00000492117.1:n.4530A>G
ENST00000541639.5:c.4578A>G	ENSP00000444293.1:p.Thr1526=
NM_001146705.1:c.4578A>G	NP_001140177.1:p.Thr1526=
NM_001146706.1:c.4314A>G	NP_001140178.1:p.Thr1438=
NM_004653.4:c.4485A>G	NP_004644.2:p.Thr1495=
XM_005262560.1:c.4350A>G	XP_005262617.1:p.Thr1450=
XM_005262561.1:c.4254A>G	XP_005262618.1:p.Thr1418=
XM_011531468.1:c.4407A>G	XP_011529770.1:p.Thr1469=
XR_430568.2:n.5260A>G
XM_005262560.3:c.4350A>G	XP_005262617.1:p.Thr1450=
XM_005262561.3:c.4254A>G	XP_005262618.1:p.Thr1418=
XM_011531468.3:c.4407A>G	XP_011529770.1:p.Thr1469=
XM_024452495.1:c.2475A>G	XP_024308263.1:p.Thr825=
XM_024452496.1:c.2241A>G	XP_024308264.1:p.Thr747=
XR_001756009.2:n.5223A>G
XR_001756010.2:n.5191A>G
XR_001756011.2:n.5088A>G
XR_001756012.2:n.5236A>G
XR_001756013.2:n.4554A>G
XR_002958832.1:n.4808A>G
XR_002958834.1:n.4879A>G
XR_002958835.1:n.4762A>G
XR_002958836.1:n.5413A>G
XR_002958837.1:n.5220A>G
XR_244571.4:n.4740A>G
XR_430568.4:n.5259A>G
NM_001146706.2:c.4314A>G	NP_001140178.1:p.Thr1438=
NM_004653.5:c.4485A>G MANE Select	NP_004644.2:p.Thr1495=
NM_001146705.2:c.4578A>G	NP_001140177.1:p.Thr1526=