Canonical Allele Identifier: CA414840092

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21867976T>C (hg19) ; chrY:g.19706090T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706090T>C , CM000686.2:g.19706090T>C	GRCh38
NC_000024.9:g.21867976T>C , CM000686.1:g.21867976T>C	GRCh37
NC_000024.8:g.20327364T>C	NCBI36
NG_032920.1:g.43850A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4525A>G MANE Select	ENSP00000322408.4:p.Asn1509Asp
ENST00000317961.8:c.4525A>G	ENSP00000322408.4:p.Asn1509Asp
ENST00000382806.6:c.4354A>G	ENSP00000372256.2:p.Asn1452Asp
ENST00000440077.5:c.4402A>G	ENSP00000398543.1:p.Asn1468Asp
ENST00000469599.6:n.3276A>G
ENST00000492117.1:n.4570A>G
ENST00000541639.5:c.4618A>G	ENSP00000444293.1:p.Asn1540Asp
NM_001146705.1:c.4618A>G	NP_001140177.1:p.Asn1540Asp
NM_001146706.1:c.4354A>G	NP_001140178.1:p.Asn1452Asp
NM_004653.4:c.4525A>G	NP_004644.2:p.Asn1509Asp
XM_005262560.1:c.4390A>G	XP_005262617.1:p.Asn1464Asp
XM_005262561.1:c.4294A>G	XP_005262618.1:p.Asn1432Asp
XM_011531468.1:c.4447A>G	XP_011529770.1:p.Asn1483Asp
XR_430568.2:n.5300A>G
XM_005262560.3:c.4390A>G	XP_005262617.1:p.Asn1464Asp
XM_005262561.3:c.4294A>G	XP_005262618.1:p.Asn1432Asp
XM_011531468.3:c.4447A>G	XP_011529770.1:p.Asn1483Asp
XM_024452495.1:c.2515A>G	XP_024308263.1:p.Asn839Asp
XM_024452496.1:c.2281A>G	XP_024308264.1:p.Asn761Asp
XR_001756009.2:n.5263A>G
XR_001756010.2:n.5231A>G
XR_001756011.2:n.5128A>G
XR_001756012.2:n.5276A>G
XR_001756013.2:n.4594A>G
XR_002958832.1:n.4848A>G
XR_002958834.1:n.4919A>G
XR_002958835.1:n.4802A>G
XR_002958836.1:n.5453A>G
XR_002958837.1:n.5260A>G
XR_244571.4:n.4780A>G
XR_430568.4:n.5299A>G
NM_001146706.2:c.4354A>G	NP_001140178.1:p.Asn1452Asp
NM_004653.5:c.4525A>G MANE Select	NP_004644.2:p.Asn1509Asp
NM_001146705.2:c.4618A>G	NP_001140177.1:p.Asn1540Asp