Canonical Allele Identifier: CA520160842

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869871G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707985G>A , CM000686.2:g.19707985G>A	GRCh38
NC_000024.9:g.21869871G>A , CM000686.1:g.21869871G>A	GRCh37
NC_000024.8:g.20329259G>A	NCBI36
NG_032920.1:g.41955C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.3348C>T MANE Select	ENSP00000322408.4:p.Asp1116=
ENST00000317961.8:c.3348C>T	ENSP00000322408.4:p.Asp1116=
ENST00000382806.6:c.3177C>T	ENSP00000372256.2:p.Asp1059=
ENST00000415360.1:c.264C>T	ENSP00000389433.1:p.Asp88=
ENST00000440077.5:c.3225C>T	ENSP00000398543.1:p.Asp1075=
ENST00000469599.6:n.1946C>T
ENST00000492117.1:n.3240C>T
ENST00000541639.5:c.3441C>T	ENSP00000444293.1:p.Asp1147=
NM_001146705.1:c.3441C>T	NP_001140177.1:p.Asp1147=
NM_001146706.1:c.3177C>T	NP_001140178.1:p.Asp1059=
NM_004653.4:c.3348C>T	NP_004644.2:p.Asp1116=
XM_005262560.1:c.3213C>T	XP_005262617.1:p.Asp1071=
XM_005262561.1:c.3117C>T	XP_005262618.1:p.Asp1039=
XM_011531468.1:c.3270C>T	XP_011529770.1:p.Asp1090=
XR_244571.2:n.3636C>T
XR_430568.2:n.3970C>T
XM_005262560.3:c.3213C>T	XP_005262617.1:p.Asp1071=
XM_005262561.3:c.3117C>T	XP_005262618.1:p.Asp1039=
XM_011531468.3:c.3270C>T	XP_011529770.1:p.Asp1090=
XM_024452495.1:c.1338C>T	XP_024308263.1:p.Asp446=
XM_024452496.1:c.1104C>T	XP_024308264.1:p.Asp368=
XR_001756009.2:n.4086C>T
XR_001756010.2:n.4086C>T
XR_001756011.2:n.3951C>T
XR_001756012.2:n.4099C>T
XR_001756013.2:n.3417C>T
XR_002958832.1:n.3518C>T
XR_002958834.1:n.3742C>T
XR_002958835.1:n.3625C>T
XR_002958836.1:n.4308C>T
XR_002958837.1:n.4115C>T
XR_244571.4:n.3635C>T
XR_430568.4:n.3969C>T
NM_001146706.2:c.3177C>T	NP_001140178.1:p.Asp1059=
NM_004653.5:c.3348C>T MANE Select	NP_004644.2:p.Asp1116=
NM_001146705.2:c.3441C>T	NP_001140177.1:p.Asp1147=