Canonical Allele Identifier: CA414844772

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869951A>G (hg19) ; chrY:g.19708065A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708065A>G , CM000686.2:g.19708065A>G	GRCh38
NC_000024.9:g.21869951A>G , CM000686.1:g.21869951A>G	GRCh37
NC_000024.8:g.20329339A>G	NCBI36
NG_032920.1:g.41875T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3268T>C MANE Select	ENSP00000322408.4:p.Cys1090Arg
ENST00000317961.8:c.3268T>C	ENSP00000322408.4:p.Cys1090Arg
ENST00000382806.6:c.3097T>C	ENSP00000372256.2:p.Cys1033Arg
ENST00000415360.1:c.184T>C	ENSP00000389433.1:p.Cys62Arg
ENST00000440077.5:c.3145T>C	ENSP00000398543.1:p.Cys1049Arg
ENST00000469599.6:n.1866T>C
ENST00000492117.1:n.3160T>C
ENST00000541639.5:c.3361T>C	ENSP00000444293.1:p.Cys1121Arg
NM_001146705.1:c.3361T>C	NP_001140177.1:p.Cys1121Arg
NM_001146706.1:c.3097T>C	NP_001140178.1:p.Cys1033Arg
NM_004653.4:c.3268T>C	NP_004644.2:p.Cys1090Arg
XM_005262560.1:c.3133T>C	XP_005262617.1:p.Cys1045Arg
XM_005262561.1:c.3037T>C	XP_005262618.1:p.Cys1013Arg
XM_011531468.1:c.3190T>C	XP_011529770.1:p.Cys1064Arg
XR_244571.2:n.3556T>C
XR_430568.2:n.3890T>C
XM_005262560.3:c.3133T>C	XP_005262617.1:p.Cys1045Arg
XM_005262561.3:c.3037T>C	XP_005262618.1:p.Cys1013Arg
XM_011531468.3:c.3190T>C	XP_011529770.1:p.Cys1064Arg
XM_024452495.1:c.1258T>C	XP_024308263.1:p.Cys420Arg
XM_024452496.1:c.1024T>C	XP_024308264.1:p.Cys342Arg
XR_001756009.2:n.4006T>C
XR_001756010.2:n.4006T>C
XR_001756011.2:n.3871T>C
XR_001756012.2:n.4019T>C
XR_001756013.2:n.3337T>C
XR_002958832.1:n.3438T>C
XR_002958834.1:n.3662T>C
XR_002958835.1:n.3545T>C
XR_002958836.1:n.4228T>C
XR_002958837.1:n.4035T>C
XR_244571.4:n.3555T>C
XR_430568.4:n.3889T>C
NM_001146706.2:c.3097T>C	NP_001140178.1:p.Cys1033Arg
NM_004653.5:c.3268T>C MANE Select	NP_004644.2:p.Cys1090Arg
NM_001146705.2:c.3361T>C	NP_001140177.1:p.Cys1121Arg