Canonical Allele Identifier: CA520514849

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868055A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706169A>G , CM000686.2:g.19706169A>G	GRCh38
NC_000024.9:g.21868055A>G , CM000686.1:g.21868055A>G	GRCh37
NC_000024.8:g.20327443A>G	NCBI36
NG_032920.1:g.43771T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4446T>C MANE Select	ENSP00000322408.4:p.His1482=
ENST00000317961.8:c.4446T>C	ENSP00000322408.4:p.His1482=
ENST00000382806.6:c.4275T>C	ENSP00000372256.2:p.His1425=
ENST00000440077.5:c.4323T>C	ENSP00000398543.1:p.His1441=
ENST00000469599.6:n.3197T>C
ENST00000492117.1:n.4491T>C
ENST00000541639.5:c.4539T>C	ENSP00000444293.1:p.His1513=
NM_001146705.1:c.4539T>C	NP_001140177.1:p.His1513=
NM_001146706.1:c.4275T>C	NP_001140178.1:p.His1425=
NM_004653.4:c.4446T>C	NP_004644.2:p.His1482=
XM_005262560.1:c.4311T>C	XP_005262617.1:p.His1437=
XM_005262561.1:c.4215T>C	XP_005262618.1:p.His1405=
XM_011531468.1:c.4368T>C	XP_011529770.1:p.His1456=
XR_430568.2:n.5221T>C
XM_005262560.3:c.4311T>C	XP_005262617.1:p.His1437=
XM_005262561.3:c.4215T>C	XP_005262618.1:p.His1405=
XM_011531468.3:c.4368T>C	XP_011529770.1:p.His1456=
XM_024452495.1:c.2436T>C	XP_024308263.1:p.His812=
XM_024452496.1:c.2202T>C	XP_024308264.1:p.His734=
XR_001756009.2:n.5184T>C
XR_001756010.2:n.5152T>C
XR_001756011.2:n.5049T>C
XR_001756012.2:n.5197T>C
XR_001756013.2:n.4515T>C
XR_002958832.1:n.4769T>C
XR_002958834.1:n.4840T>C
XR_002958835.1:n.4723T>C
XR_002958836.1:n.5374T>C
XR_002958837.1:n.5181T>C
XR_244571.4:n.4701T>C
XR_430568.4:n.5220T>C
NM_001146706.2:c.4275T>C	NP_001140178.1:p.His1425=
NM_004653.5:c.4446T>C MANE Select	NP_004644.2:p.His1482=
NM_001146705.2:c.4539T>C	NP_001140177.1:p.His1513=