Canonical Allele Identifier: CA414843647

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869462G>T (hg19) ; chrY:g.19707576G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707576G>T , CM000686.2:g.19707576G>T	GRCh38
NC_000024.9:g.21869462G>T , CM000686.1:g.21869462G>T	GRCh37
NC_000024.8:g.20328850G>T	NCBI36
NG_032920.1:g.42364C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3570C>A MANE Select	ENSP00000322408.4:p.Asp1190Glu
ENST00000317961.8:c.3570C>A	ENSP00000322408.4:p.Asp1190Glu
ENST00000382806.6:c.3399C>A	ENSP00000372256.2:p.Asp1133Glu
ENST00000415360.1:c.486C>A	ENSP00000389433.1:p.Asp162Glu
ENST00000440077.5:c.3447C>A	ENSP00000398543.1:p.Asp1149Glu
ENST00000469599.6:n.2168C>A
ENST00000492117.1:n.3462C>A
ENST00000541639.5:c.3663C>A	ENSP00000444293.1:p.Asp1221Glu
NM_001146705.1:c.3663C>A	NP_001140177.1:p.Asp1221Glu
NM_001146706.1:c.3399C>A	NP_001140178.1:p.Asp1133Glu
NM_004653.4:c.3570C>A	NP_004644.2:p.Asp1190Glu
XM_005262560.1:c.3435C>A	XP_005262617.1:p.Asp1145Glu
XM_005262561.1:c.3339C>A	XP_005262618.1:p.Asp1113Glu
XM_011531468.1:c.3492C>A	XP_011529770.1:p.Asp1164Glu
XR_244571.2:n.3858C>A
XR_430568.2:n.4192C>A
XM_005262560.3:c.3435C>A	XP_005262617.1:p.Asp1145Glu
XM_005262561.3:c.3339C>A	XP_005262618.1:p.Asp1113Glu
XM_011531468.3:c.3492C>A	XP_011529770.1:p.Asp1164Glu
XM_024452495.1:c.1560C>A	XP_024308263.1:p.Asp520Glu
XM_024452496.1:c.1326C>A	XP_024308264.1:p.Asp442Glu
XR_001756009.2:n.4308C>A
XR_001756010.2:n.4308C>A
XR_001756011.2:n.4173C>A
XR_001756012.2:n.4321C>A
XR_001756013.2:n.3639C>A
XR_002958832.1:n.3740C>A
XR_002958834.1:n.3964C>A
XR_002958835.1:n.3847C>A
XR_002958836.1:n.4530C>A
XR_002958837.1:n.4337C>A
XR_244571.4:n.3857C>A
XR_430568.4:n.4191C>A
NM_001146706.2:c.3399C>A	NP_001140178.1:p.Asp1133Glu
NM_004653.5:c.3570C>A MANE Select	NP_004644.2:p.Asp1190Glu
NM_001146705.2:c.3663C>A	NP_001140177.1:p.Asp1221Glu