Canonical Allele Identifier: CA2470918778

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706170T= , CM000686.2:g.19706170T=	GRCh38
NC_000024.9:g.21868056T= , CM000686.1:g.21868056T=	GRCh37
NC_000024.8:g.20327444T=	NCBI36
NG_032920.1:g.43770A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4445A= MANE Select	ENSP00000322408.4:p.His1482=
ENST00000317961.8:c.4445A=	ENSP00000322408.4:p.His1482=
ENST00000382806.6:c.4274A=	ENSP00000372256.2:p.His1425=
ENST00000440077.5:c.4322A=	ENSP00000398543.1:p.His1441=
ENST00000469599.6:n.3196A=
ENST00000492117.1:n.4490A=
ENST00000541639.5:c.4538A=	ENSP00000444293.1:p.His1513=
NM_001146705.1:c.4538A=	NP_001140177.1:p.His1513=
NM_001146706.1:c.4274A=	NP_001140178.1:p.His1425=
NM_004653.4:c.4445A=	NP_004644.2:p.His1482=
XM_005262560.1:c.4310A=	XP_005262617.1:p.His1437=
XM_005262561.1:c.4214A=	XP_005262618.1:p.His1405=
XM_011531468.1:c.4367A=	XP_011529770.1:p.His1456=
XR_430568.2:n.5220A=
XM_005262560.3:c.4310A=	XP_005262617.1:p.His1437=
XM_005262561.3:c.4214A=	XP_005262618.1:p.His1405=
XM_011531468.3:c.4367A=	XP_011529770.1:p.His1456=
XM_024452495.1:c.2435A=	XP_024308263.1:p.His812=
XM_024452496.1:c.2201A=	XP_024308264.1:p.His734=
XR_001756009.2:n.5183A=
XR_001756010.2:n.5151A=
XR_001756011.2:n.5048A=
XR_001756012.2:n.5196A=
XR_001756013.2:n.4514A=
XR_002958832.1:n.4768A=
XR_002958834.1:n.4839A=
XR_002958835.1:n.4722A=
XR_002958836.1:n.5373A=
XR_002958837.1:n.5180A=
XR_244571.4:n.4700A=
XR_430568.4:n.5219A=
NM_001146706.2:c.4274A=	NP_001140178.1:p.His1425=
NM_004653.5:c.4445A= MANE Select	NP_004644.2:p.His1482=
NM_001146705.2:c.4538A=	NP_001140177.1:p.His1513=