Canonical Allele Identifier: CA520159922

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868693T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706807T>G , CM000686.2:g.19706807T>G	GRCh38
NC_000024.9:g.21868693T>G , CM000686.1:g.21868693T>G	GRCh37
NC_000024.8:g.20328081T>G	NCBI36
NG_032920.1:g.43133A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4056A>C MANE Select	ENSP00000322408.4:p.Pro1352=
ENST00000317961.8:c.4056A>C	ENSP00000322408.4:p.Pro1352=
ENST00000382806.6:c.3885A>C	ENSP00000372256.2:p.Pro1295=
ENST00000440077.5:c.3933A>C	ENSP00000398543.1:p.Pro1311=
ENST00000469599.6:n.2654A>C
ENST00000492117.1:n.3948A>C
ENST00000541639.5:c.4149A>C	ENSP00000444293.1:p.Pro1383=
NM_001146705.1:c.4149A>C	NP_001140177.1:p.Pro1383=
NM_001146706.1:c.3885A>C	NP_001140178.1:p.Pro1295=
NM_004653.4:c.4056A>C	NP_004644.2:p.Pro1352=
XM_005262560.1:c.3921A>C	XP_005262617.1:p.Pro1307=
XM_005262561.1:c.3825A>C	XP_005262618.1:p.Pro1275=
XM_011531468.1:c.3978A>C	XP_011529770.1:p.Pro1326=
XR_244571.2:n.4344A>C
XR_430568.2:n.4678A>C
XM_005262560.3:c.3921A>C	XP_005262617.1:p.Pro1307=
XM_005262561.3:c.3825A>C	XP_005262618.1:p.Pro1275=
XM_011531468.3:c.3978A>C	XP_011529770.1:p.Pro1326=
XM_024452495.1:c.2046A>C	XP_024308263.1:p.Pro682=
XM_024452496.1:c.1812A>C	XP_024308264.1:p.Pro604=
XR_001756009.2:n.4794A>C
XR_001756010.2:n.4794A>C
XR_001756011.2:n.4659A>C
XR_001756012.2:n.4807A>C
XR_001756013.2:n.4125A>C
XR_002958832.1:n.4226A>C
XR_002958834.1:n.4450A>C
XR_002958835.1:n.4333A>C
XR_002958836.1:n.5016A>C
XR_002958837.1:n.4823A>C
XR_244571.4:n.4343A>C
XR_430568.4:n.4677A>C
NM_001146706.2:c.3885A>C	NP_001140178.1:p.Pro1295=
NM_004653.5:c.4056A>C MANE Select	NP_004644.2:p.Pro1352=
NM_001146705.2:c.4149A>C	NP_001140177.1:p.Pro1383=