Canonical Allele Identifier: CA520516607

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869417A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707531A>G , CM000686.2:g.19707531A>G	GRCh38
NC_000024.9:g.21869417A>G , CM000686.1:g.21869417A>G	GRCh37
NC_000024.8:g.20328805A>G	NCBI36
NG_032920.1:g.42409T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3615T>C MANE Select	ENSP00000322408.4:p.His1205=
ENST00000317961.8:c.3615T>C	ENSP00000322408.4:p.His1205=
ENST00000382806.6:c.3444T>C	ENSP00000372256.2:p.His1148=
ENST00000415360.1:c.531T>C	ENSP00000389433.1:p.His177=
ENST00000440077.5:c.3492T>C	ENSP00000398543.1:p.His1164=
ENST00000469599.6:n.2213T>C
ENST00000492117.1:n.3507T>C
ENST00000541639.5:c.3708T>C	ENSP00000444293.1:p.His1236=
NM_001146705.1:c.3708T>C	NP_001140177.1:p.His1236=
NM_001146706.1:c.3444T>C	NP_001140178.1:p.His1148=
NM_004653.4:c.3615T>C	NP_004644.2:p.His1205=
XM_005262560.1:c.3480T>C	XP_005262617.1:p.His1160=
XM_005262561.1:c.3384T>C	XP_005262618.1:p.His1128=
XM_011531468.1:c.3537T>C	XP_011529770.1:p.His1179=
XR_244571.2:n.3903T>C
XR_430568.2:n.4237T>C
XM_005262560.3:c.3480T>C	XP_005262617.1:p.His1160=
XM_005262561.3:c.3384T>C	XP_005262618.1:p.His1128=
XM_011531468.3:c.3537T>C	XP_011529770.1:p.His1179=
XM_024452495.1:c.1605T>C	XP_024308263.1:p.His535=
XM_024452496.1:c.1371T>C	XP_024308264.1:p.His457=
XR_001756009.2:n.4353T>C
XR_001756010.2:n.4353T>C
XR_001756011.2:n.4218T>C
XR_001756012.2:n.4366T>C
XR_001756013.2:n.3684T>C
XR_002958832.1:n.3785T>C
XR_002958834.1:n.4009T>C
XR_002958835.1:n.3892T>C
XR_002958836.1:n.4575T>C
XR_002958837.1:n.4382T>C
XR_244571.4:n.3902T>C
XR_430568.4:n.4236T>C
NM_001146706.2:c.3444T>C	NP_001140178.1:p.His1148=
NM_004653.5:c.3615T>C MANE Select	NP_004644.2:p.His1205=
NM_001146705.2:c.3708T>C	NP_001140177.1:p.His1236=