Canonical Allele Identifier: CA414842028

Gene: KDM5D

Linked Data

• gnomAD v3: Y-19732698-A-C
• gnomAD v4: Y-19732698-A-C
• MyVariant Identifiers: chrY:g.21894584A>C (hg19) ; chrY:g.19732698A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19732698A>C , CM000686.2:g.19732698A>C	GRCh38
NC_000024.9:g.21894584A>C , CM000686.1:g.21894584A>C	GRCh37
NC_000024.8:g.20353972A>C	NCBI36
NG_032920.1:g.17242T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.978T>G MANE Select	ENSP00000322408.4:p.Asp326Glu
ENST00000317961.8:c.978T>G	ENSP00000322408.4:p.Asp326Glu
ENST00000382806.6:c.807T>G	ENSP00000372256.2:p.Asp269Glu
ENST00000440077.5:c.855T>G	ENSP00000398543.1:p.Asp285Glu
ENST00000447300.1:c.843T>G	ENSP00000416377.1:p.Asp281Glu
ENST00000541639.5:c.978T>G	ENSP00000444293.1:p.Asp326Glu
NM_001146705.1:c.978T>G	NP_001140177.1:p.Asp326Glu
NM_001146706.1:c.807T>G	NP_001140178.1:p.Asp269Glu
NM_004653.4:c.978T>G	NP_004644.2:p.Asp326Glu
XM_005262560.1:c.843T>G	XP_005262617.1:p.Asp281Glu
XM_005262561.1:c.978T>G	XP_005262618.1:p.Asp326Glu
XM_005262562.2:c.978T>G	XP_005262619.1:p.Asp326Glu
XM_011531468.1:c.978T>G	XP_011529770.1:p.Asp326Glu
XR_244571.2:n.1266T>G
XR_430568.2:n.1266T>G
XR_938609.1:n.1266T>G
XR_938610.1:n.1266T>G
XM_005262560.3:c.843T>G	XP_005262617.1:p.Asp281Glu
XM_005262561.3:c.978T>G	XP_005262618.1:p.Asp326Glu
XM_011531468.3:c.978T>G	XP_011529770.1:p.Asp326Glu
XM_024452495.1:c.-1140T>G	XP_024308263.1:n.-1140T>G
XR_001756009.2:n.1265T>G
XR_001756010.2:n.1265T>G
XR_001756011.2:n.1130T>G
XR_001756012.2:n.1265T>G
XR_001756013.2:n.1265T>G
XR_002958832.1:n.1265T>G
XR_002958833.1:n.1265T>G
XR_002958834.1:n.1265T>G
XR_002958835.1:n.1265T>G
XR_002958836.1:n.1265T>G
XR_002958837.1:n.1265T>G
XR_244571.4:n.1265T>G
XR_430568.4:n.1265T>G
NM_001146706.2:c.807T>G	NP_001140178.1:p.Asp269Glu
NM_004653.5:c.978T>G MANE Select	NP_004644.2:p.Asp326Glu
NM_001146705.2:c.978T>G	NP_001140177.1:p.Asp326Glu