Canonical Allele Identifier: CA520159434

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21867983T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706097T>C , CM000686.2:g.19706097T>C	GRCh38
NC_000024.9:g.21867983T>C , CM000686.1:g.21867983T>C	GRCh37
NC_000024.8:g.20327371T>C	NCBI36
NG_032920.1:g.43843A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4518A>G MANE Select	ENSP00000322408.4:p.Gly1506=
ENST00000317961.8:c.4518A>G	ENSP00000322408.4:p.Gly1506=
ENST00000382806.6:c.4347A>G	ENSP00000372256.2:p.Gly1449=
ENST00000440077.5:c.4395A>G	ENSP00000398543.1:p.Gly1465=
ENST00000469599.6:n.3269A>G
ENST00000492117.1:n.4563A>G
ENST00000541639.5:c.4611A>G	ENSP00000444293.1:p.Gly1537=
NM_001146705.1:c.4611A>G	NP_001140177.1:p.Gly1537=
NM_001146706.1:c.4347A>G	NP_001140178.1:p.Gly1449=
NM_004653.4:c.4518A>G	NP_004644.2:p.Gly1506=
XM_005262560.1:c.4383A>G	XP_005262617.1:p.Gly1461=
XM_005262561.1:c.4287A>G	XP_005262618.1:p.Gly1429=
XM_011531468.1:c.4440A>G	XP_011529770.1:p.Gly1480=
XR_430568.2:n.5293A>G
XM_005262560.3:c.4383A>G	XP_005262617.1:p.Gly1461=
XM_005262561.3:c.4287A>G	XP_005262618.1:p.Gly1429=
XM_011531468.3:c.4440A>G	XP_011529770.1:p.Gly1480=
XM_024452495.1:c.2508A>G	XP_024308263.1:p.Gly836=
XM_024452496.1:c.2274A>G	XP_024308264.1:p.Gly758=
XR_001756009.2:n.5256A>G
XR_001756010.2:n.5224A>G
XR_001756011.2:n.5121A>G
XR_001756012.2:n.5269A>G
XR_001756013.2:n.4587A>G
XR_002958832.1:n.4841A>G
XR_002958834.1:n.4912A>G
XR_002958835.1:n.4795A>G
XR_002958836.1:n.5446A>G
XR_002958837.1:n.5253A>G
XR_244571.4:n.4773A>G
XR_430568.4:n.5292A>G
NM_001146706.2:c.4347A>G	NP_001140178.1:p.Gly1449=
NM_004653.5:c.4518A>G MANE Select	NP_004644.2:p.Gly1506=
NM_001146705.2:c.4611A>G	NP_001140177.1:p.Gly1537=