Canonical Allele Identifier: CA520160865

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869913A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708027A>C , CM000686.2:g.19708027A>C	GRCh38
NC_000024.9:g.21869913A>C , CM000686.1:g.21869913A>C	GRCh37
NC_000024.8:g.20329301A>C	NCBI36
NG_032920.1:g.41913T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3306T>G MANE Select	ENSP00000322408.4:p.Arg1102=
ENST00000317961.8:c.3306T>G	ENSP00000322408.4:p.Arg1102=
ENST00000382806.6:c.3135T>G	ENSP00000372256.2:p.Arg1045=
ENST00000415360.1:c.222T>G	ENSP00000389433.1:p.Arg74=
ENST00000440077.5:c.3183T>G	ENSP00000398543.1:p.Arg1061=
ENST00000469599.6:n.1904T>G
ENST00000492117.1:n.3198T>G
ENST00000541639.5:c.3399T>G	ENSP00000444293.1:p.Arg1133=
NM_001146705.1:c.3399T>G	NP_001140177.1:p.Arg1133=
NM_001146706.1:c.3135T>G	NP_001140178.1:p.Arg1045=
NM_004653.4:c.3306T>G	NP_004644.2:p.Arg1102=
XM_005262560.1:c.3171T>G	XP_005262617.1:p.Arg1057=
XM_005262561.1:c.3075T>G	XP_005262618.1:p.Arg1025=
XM_011531468.1:c.3228T>G	XP_011529770.1:p.Arg1076=
XR_244571.2:n.3594T>G
XR_430568.2:n.3928T>G
XM_005262560.3:c.3171T>G	XP_005262617.1:p.Arg1057=
XM_005262561.3:c.3075T>G	XP_005262618.1:p.Arg1025=
XM_011531468.3:c.3228T>G	XP_011529770.1:p.Arg1076=
XM_024452495.1:c.1296T>G	XP_024308263.1:p.Arg432=
XM_024452496.1:c.1062T>G	XP_024308264.1:p.Arg354=
XR_001756009.2:n.4044T>G
XR_001756010.2:n.4044T>G
XR_001756011.2:n.3909T>G
XR_001756012.2:n.4057T>G
XR_001756013.2:n.3375T>G
XR_002958832.1:n.3476T>G
XR_002958834.1:n.3700T>G
XR_002958835.1:n.3583T>G
XR_002958836.1:n.4266T>G
XR_002958837.1:n.4073T>G
XR_244571.4:n.3593T>G
XR_430568.4:n.3927T>G
NM_001146706.2:c.3135T>G	NP_001140178.1:p.Arg1045=
NM_004653.5:c.3306T>G MANE Select	NP_004644.2:p.Arg1102=
NM_001146705.2:c.3399T>G	NP_001140177.1:p.Arg1133=