Canonical Allele Identifier: CA414844324

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869846G>T (hg19) ; chrY:g.19707960G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707960G>T , CM000686.2:g.19707960G>T	GRCh38
NC_000024.9:g.21869846G>T , CM000686.1:g.21869846G>T	GRCh37
NC_000024.8:g.20329234G>T	NCBI36
NG_032920.1:g.41980C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3373C>A MANE Select	ENSP00000322408.4:p.Gln1125Lys
ENST00000317961.8:c.3373C>A	ENSP00000322408.4:p.Gln1125Lys
ENST00000382806.6:c.3202C>A	ENSP00000372256.2:p.Gln1068Lys
ENST00000415360.1:c.289C>A	ENSP00000389433.1:p.Gln97Lys
ENST00000440077.5:c.3250C>A	ENSP00000398543.1:p.Gln1084Lys
ENST00000469599.6:n.1971C>A
ENST00000492117.1:n.3265C>A
ENST00000541639.5:c.3466C>A	ENSP00000444293.1:p.Gln1156Lys
NM_001146705.1:c.3466C>A	NP_001140177.1:p.Gln1156Lys
NM_001146706.1:c.3202C>A	NP_001140178.1:p.Gln1068Lys
NM_004653.4:c.3373C>A	NP_004644.2:p.Gln1125Lys
XM_005262560.1:c.3238C>A	XP_005262617.1:p.Gln1080Lys
XM_005262561.1:c.3142C>A	XP_005262618.1:p.Gln1048Lys
XM_011531468.1:c.3295C>A	XP_011529770.1:p.Gln1099Lys
XR_244571.2:n.3661C>A
XR_430568.2:n.3995C>A
XM_005262560.3:c.3238C>A	XP_005262617.1:p.Gln1080Lys
XM_005262561.3:c.3142C>A	XP_005262618.1:p.Gln1048Lys
XM_011531468.3:c.3295C>A	XP_011529770.1:p.Gln1099Lys
XM_024452495.1:c.1363C>A	XP_024308263.1:p.Gln455Lys
XM_024452496.1:c.1129C>A	XP_024308264.1:p.Gln377Lys
XR_001756009.2:n.4111C>A
XR_001756010.2:n.4111C>A
XR_001756011.2:n.3976C>A
XR_001756012.2:n.4124C>A
XR_001756013.2:n.3442C>A
XR_002958832.1:n.3543C>A
XR_002958834.1:n.3767C>A
XR_002958835.1:n.3650C>A
XR_002958836.1:n.4333C>A
XR_002958837.1:n.4140C>A
XR_244571.4:n.3660C>A
XR_430568.4:n.3994C>A
NM_001146706.2:c.3202C>A	NP_001140178.1:p.Gln1068Lys
NM_004653.5:c.3373C>A MANE Select	NP_004644.2:p.Gln1125Lys
NM_001146705.2:c.3466C>A	NP_001140177.1:p.Gln1156Lys