Canonical Allele Identifier: CA520516968

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869543T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707657T>C , CM000686.2:g.19707657T>C	GRCh38
NC_000024.9:g.21869543T>C , CM000686.1:g.21869543T>C	GRCh37
NC_000024.8:g.20328931T>C	NCBI36
NG_032920.1:g.42283A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3489A>G MANE Select	ENSP00000322408.4:p.Ala1163=
ENST00000317961.8:c.3489A>G	ENSP00000322408.4:p.Ala1163=
ENST00000382806.6:c.3318A>G	ENSP00000372256.2:p.Ala1106=
ENST00000415360.1:c.405A>G	ENSP00000389433.1:p.Ala135=
ENST00000440077.5:c.3366A>G	ENSP00000398543.1:p.Ala1122=
ENST00000469599.6:n.2087A>G
ENST00000492117.1:n.3381A>G
ENST00000541639.5:c.3582A>G	ENSP00000444293.1:p.Ala1194=
NM_001146705.1:c.3582A>G	NP_001140177.1:p.Ala1194=
NM_001146706.1:c.3318A>G	NP_001140178.1:p.Ala1106=
NM_004653.4:c.3489A>G	NP_004644.2:p.Ala1163=
XM_005262560.1:c.3354A>G	XP_005262617.1:p.Ala1118=
XM_005262561.1:c.3258A>G	XP_005262618.1:p.Ala1086=
XM_011531468.1:c.3411A>G	XP_011529770.1:p.Ala1137=
XR_244571.2:n.3777A>G
XR_430568.2:n.4111A>G
XM_005262560.3:c.3354A>G	XP_005262617.1:p.Ala1118=
XM_005262561.3:c.3258A>G	XP_005262618.1:p.Ala1086=
XM_011531468.3:c.3411A>G	XP_011529770.1:p.Ala1137=
XM_024452495.1:c.1479A>G	XP_024308263.1:p.Ala493=
XM_024452496.1:c.1245A>G	XP_024308264.1:p.Ala415=
XR_001756009.2:n.4227A>G
XR_001756010.2:n.4227A>G
XR_001756011.2:n.4092A>G
XR_001756012.2:n.4240A>G
XR_001756013.2:n.3558A>G
XR_002958832.1:n.3659A>G
XR_002958834.1:n.3883A>G
XR_002958835.1:n.3766A>G
XR_002958836.1:n.4449A>G
XR_002958837.1:n.4256A>G
XR_244571.4:n.3776A>G
XR_430568.4:n.4110A>G
NM_001146706.2:c.3318A>G	NP_001140178.1:p.Ala1106=
NM_004653.5:c.3489A>G MANE Select	NP_004644.2:p.Ala1163=
NM_001146705.2:c.3582A>G	NP_001140177.1:p.Ala1194=