Canonical Allele Identifier: CA520160758

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869573G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707687G>A , CM000686.2:g.19707687G>A	GRCh38
NC_000024.9:g.21869573G>A , CM000686.1:g.21869573G>A	GRCh37
NC_000024.8:g.20328961G>A	NCBI36
NG_032920.1:g.42253C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3459C>T MANE Select	ENSP00000322408.4:p.Arg1153=
ENST00000317961.8:c.3459C>T	ENSP00000322408.4:p.Arg1153=
ENST00000382806.6:c.3288C>T	ENSP00000372256.2:p.Arg1096=
ENST00000415360.1:c.375C>T	ENSP00000389433.1:p.Arg125=
ENST00000440077.5:c.3336C>T	ENSP00000398543.1:p.Arg1112=
ENST00000469599.6:n.2057C>T
ENST00000492117.1:n.3351C>T
ENST00000541639.5:c.3552C>T	ENSP00000444293.1:p.Arg1184=
NM_001146705.1:c.3552C>T	NP_001140177.1:p.Arg1184=
NM_001146706.1:c.3288C>T	NP_001140178.1:p.Arg1096=
NM_004653.4:c.3459C>T	NP_004644.2:p.Arg1153=
XM_005262560.1:c.3324C>T	XP_005262617.1:p.Arg1108=
XM_005262561.1:c.3228C>T	XP_005262618.1:p.Arg1076=
XM_011531468.1:c.3381C>T	XP_011529770.1:p.Arg1127=
XR_244571.2:n.3747C>T
XR_430568.2:n.4081C>T
XM_005262560.3:c.3324C>T	XP_005262617.1:p.Arg1108=
XM_005262561.3:c.3228C>T	XP_005262618.1:p.Arg1076=
XM_011531468.3:c.3381C>T	XP_011529770.1:p.Arg1127=
XM_024452495.1:c.1449C>T	XP_024308263.1:p.Arg483=
XM_024452496.1:c.1215C>T	XP_024308264.1:p.Arg405=
XR_001756009.2:n.4197C>T
XR_001756010.2:n.4197C>T
XR_001756011.2:n.4062C>T
XR_001756012.2:n.4210C>T
XR_001756013.2:n.3528C>T
XR_002958832.1:n.3629C>T
XR_002958834.1:n.3853C>T
XR_002958835.1:n.3736C>T
XR_002958836.1:n.4419C>T
XR_002958837.1:n.4226C>T
XR_244571.4:n.3746C>T
XR_430568.4:n.4080C>T
NM_001146706.2:c.3288C>T	NP_001140178.1:p.Arg1096=
NM_004653.5:c.3459C>T MANE Select	NP_004644.2:p.Arg1153=
NM_001146705.2:c.3552C>T	NP_001140177.1:p.Arg1184=