Canonical Allele Identifier: CA414844688

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869932C>T (hg19) ; chrY:g.19708046C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708046C>T , CM000686.2:g.19708046C>T	GRCh38
NC_000024.9:g.21869932C>T , CM000686.1:g.21869932C>T	GRCh37
NC_000024.8:g.20329320C>T	NCBI36
NG_032920.1:g.41894G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3287G>A MANE Select	ENSP00000322408.4:p.Gly1096Asp
ENST00000317961.8:c.3287G>A	ENSP00000322408.4:p.Gly1096Asp
ENST00000382806.6:c.3116G>A	ENSP00000372256.2:p.Gly1039Asp
ENST00000415360.1:c.203G>A	ENSP00000389433.1:p.Gly68Asp
ENST00000440077.5:c.3164G>A	ENSP00000398543.1:p.Gly1055Asp
ENST00000469599.6:n.1885G>A
ENST00000492117.1:n.3179G>A
ENST00000541639.5:c.3380G>A	ENSP00000444293.1:p.Gly1127Asp
NM_001146705.1:c.3380G>A	NP_001140177.1:p.Gly1127Asp
NM_001146706.1:c.3116G>A	NP_001140178.1:p.Gly1039Asp
NM_004653.4:c.3287G>A	NP_004644.2:p.Gly1096Asp
XM_005262560.1:c.3152G>A	XP_005262617.1:p.Gly1051Asp
XM_005262561.1:c.3056G>A	XP_005262618.1:p.Gly1019Asp
XM_011531468.1:c.3209G>A	XP_011529770.1:p.Gly1070Asp
XR_244571.2:n.3575G>A
XR_430568.2:n.3909G>A
XM_005262560.3:c.3152G>A	XP_005262617.1:p.Gly1051Asp
XM_005262561.3:c.3056G>A	XP_005262618.1:p.Gly1019Asp
XM_011531468.3:c.3209G>A	XP_011529770.1:p.Gly1070Asp
XM_024452495.1:c.1277G>A	XP_024308263.1:p.Gly426Asp
XM_024452496.1:c.1043G>A	XP_024308264.1:p.Gly348Asp
XR_001756009.2:n.4025G>A
XR_001756010.2:n.4025G>A
XR_001756011.2:n.3890G>A
XR_001756012.2:n.4038G>A
XR_001756013.2:n.3356G>A
XR_002958832.1:n.3457G>A
XR_002958834.1:n.3681G>A
XR_002958835.1:n.3564G>A
XR_002958836.1:n.4247G>A
XR_002958837.1:n.4054G>A
XR_244571.4:n.3574G>A
XR_430568.4:n.3908G>A
NM_001146706.2:c.3116G>A	NP_001140178.1:p.Gly1039Asp
NM_004653.5:c.3287G>A MANE Select	NP_004644.2:p.Gly1096Asp
NM_001146705.2:c.3380G>A	NP_001140177.1:p.Gly1127Asp