Canonical Allele Identifier: CA520516460

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869339A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707453A>G , CM000686.2:g.19707453A>G	GRCh38
NC_000024.9:g.21869339A>G , CM000686.1:g.21869339A>G	GRCh37
NC_000024.8:g.20328727A>G	NCBI36
NG_032920.1:g.42487T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3693T>C MANE Select	ENSP00000322408.4:p.Cys1231=
ENST00000317961.8:c.3693T>C	ENSP00000322408.4:p.Cys1231=
ENST00000382806.6:c.3522T>C	ENSP00000372256.2:p.Cys1174=
ENST00000415360.1:c.609T>C	ENSP00000389433.1:p.Cys203=
ENST00000440077.5:c.3570T>C	ENSP00000398543.1:p.Cys1190=
ENST00000469599.6:n.2291T>C
ENST00000492117.1:n.3585T>C
ENST00000541639.5:c.3786T>C	ENSP00000444293.1:p.Cys1262=
NM_001146705.1:c.3786T>C	NP_001140177.1:p.Cys1262=
NM_001146706.1:c.3522T>C	NP_001140178.1:p.Cys1174=
NM_004653.4:c.3693T>C	NP_004644.2:p.Cys1231=
XM_005262560.1:c.3558T>C	XP_005262617.1:p.Cys1186=
XM_005262561.1:c.3462T>C	XP_005262618.1:p.Cys1154=
XM_011531468.1:c.3615T>C	XP_011529770.1:p.Cys1205=
XR_244571.2:n.3981T>C
XR_430568.2:n.4315T>C
XM_005262560.3:c.3558T>C	XP_005262617.1:p.Cys1186=
XM_005262561.3:c.3462T>C	XP_005262618.1:p.Cys1154=
XM_011531468.3:c.3615T>C	XP_011529770.1:p.Cys1205=
XM_024452495.1:c.1683T>C	XP_024308263.1:p.Cys561=
XM_024452496.1:c.1449T>C	XP_024308264.1:p.Cys483=
XR_001756009.2:n.4431T>C
XR_001756010.2:n.4431T>C
XR_001756011.2:n.4296T>C
XR_001756012.2:n.4444T>C
XR_001756013.2:n.3762T>C
XR_002958832.1:n.3863T>C
XR_002958834.1:n.4087T>C
XR_002958835.1:n.3970T>C
XR_002958836.1:n.4653T>C
XR_002958837.1:n.4460T>C
XR_244571.4:n.3980T>C
XR_430568.4:n.4314T>C
NM_001146706.2:c.3522T>C	NP_001140178.1:p.Cys1174=
NM_004653.5:c.3693T>C MANE Select	NP_004644.2:p.Cys1231=
NM_001146705.2:c.3786T>C	NP_001140177.1:p.Cys1262=