Canonical Allele Identifier: CA414844710

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869937G>T (hg19) ; chrY:g.19708051G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708051G>T , CM000686.2:g.19708051G>T	GRCh38
NC_000024.9:g.21869937G>T , CM000686.1:g.21869937G>T	GRCh37
NC_000024.8:g.20329325G>T	NCBI36
NG_032920.1:g.41889C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3282C>A MANE Select	ENSP00000322408.4:p.Asp1094Glu
ENST00000317961.8:c.3282C>A	ENSP00000322408.4:p.Asp1094Glu
ENST00000382806.6:c.3111C>A	ENSP00000372256.2:p.Asp1037Glu
ENST00000415360.1:c.198C>A	ENSP00000389433.1:p.Asp66Glu
ENST00000440077.5:c.3159C>A	ENSP00000398543.1:p.Asp1053Glu
ENST00000469599.6:n.1880C>A
ENST00000492117.1:n.3174C>A
ENST00000541639.5:c.3375C>A	ENSP00000444293.1:p.Asp1125Glu
NM_001146705.1:c.3375C>A	NP_001140177.1:p.Asp1125Glu
NM_001146706.1:c.3111C>A	NP_001140178.1:p.Asp1037Glu
NM_004653.4:c.3282C>A	NP_004644.2:p.Asp1094Glu
XM_005262560.1:c.3147C>A	XP_005262617.1:p.Asp1049Glu
XM_005262561.1:c.3051C>A	XP_005262618.1:p.Asp1017Glu
XM_011531468.1:c.3204C>A	XP_011529770.1:p.Asp1068Glu
XR_244571.2:n.3570C>A
XR_430568.2:n.3904C>A
XM_005262560.3:c.3147C>A	XP_005262617.1:p.Asp1049Glu
XM_005262561.3:c.3051C>A	XP_005262618.1:p.Asp1017Glu
XM_011531468.3:c.3204C>A	XP_011529770.1:p.Asp1068Glu
XM_024452495.1:c.1272C>A	XP_024308263.1:p.Asp424Glu
XM_024452496.1:c.1038C>A	XP_024308264.1:p.Asp346Glu
XR_001756009.2:n.4020C>A
XR_001756010.2:n.4020C>A
XR_001756011.2:n.3885C>A
XR_001756012.2:n.4033C>A
XR_001756013.2:n.3351C>A
XR_002958832.1:n.3452C>A
XR_002958834.1:n.3676C>A
XR_002958835.1:n.3559C>A
XR_002958836.1:n.4242C>A
XR_002958837.1:n.4049C>A
XR_244571.4:n.3569C>A
XR_430568.4:n.3903C>A
NM_001146706.2:c.3111C>A	NP_001140178.1:p.Asp1037Glu
NM_004653.5:c.3282C>A MANE Select	NP_004644.2:p.Asp1094Glu
NM_001146705.2:c.3375C>A	NP_001140177.1:p.Asp1125Glu