Canonical Allele Identifier: CA520516558

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869399C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707513C>T , CM000686.2:g.19707513C>T	GRCh38
NC_000024.9:g.21869399C>T , CM000686.1:g.21869399C>T	GRCh37
NC_000024.8:g.20328787C>T	NCBI36
NG_032920.1:g.42427G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3633G>A MANE Select	ENSP00000322408.4:p.Lys1211=
ENST00000317961.8:c.3633G>A	ENSP00000322408.4:p.Lys1211=
ENST00000382806.6:c.3462G>A	ENSP00000372256.2:p.Lys1154=
ENST00000415360.1:c.549G>A	ENSP00000389433.1:p.Lys183=
ENST00000440077.5:c.3510G>A	ENSP00000398543.1:p.Lys1170=
ENST00000469599.6:n.2231G>A
ENST00000492117.1:n.3525G>A
ENST00000541639.5:c.3726G>A	ENSP00000444293.1:p.Lys1242=
NM_001146705.1:c.3726G>A	NP_001140177.1:p.Lys1242=
NM_001146706.1:c.3462G>A	NP_001140178.1:p.Lys1154=
NM_004653.4:c.3633G>A	NP_004644.2:p.Lys1211=
XM_005262560.1:c.3498G>A	XP_005262617.1:p.Lys1166=
XM_005262561.1:c.3402G>A	XP_005262618.1:p.Lys1134=
XM_011531468.1:c.3555G>A	XP_011529770.1:p.Lys1185=
XR_244571.2:n.3921G>A
XR_430568.2:n.4255G>A
XM_005262560.3:c.3498G>A	XP_005262617.1:p.Lys1166=
XM_005262561.3:c.3402G>A	XP_005262618.1:p.Lys1134=
XM_011531468.3:c.3555G>A	XP_011529770.1:p.Lys1185=
XM_024452495.1:c.1623G>A	XP_024308263.1:p.Lys541=
XM_024452496.1:c.1389G>A	XP_024308264.1:p.Lys463=
XR_001756009.2:n.4371G>A
XR_001756010.2:n.4371G>A
XR_001756011.2:n.4236G>A
XR_001756012.2:n.4384G>A
XR_001756013.2:n.3702G>A
XR_002958832.1:n.3803G>A
XR_002958834.1:n.4027G>A
XR_002958835.1:n.3910G>A
XR_002958836.1:n.4593G>A
XR_002958837.1:n.4400G>A
XR_244571.4:n.3920G>A
XR_430568.4:n.4254G>A
NM_001146706.2:c.3462G>A	NP_001140178.1:p.Lys1154=
NM_004653.5:c.3633G>A MANE Select	NP_004644.2:p.Lys1211=
NM_001146705.2:c.3726G>A	NP_001140177.1:p.Lys1242=