Canonical Allele Identifier: CA520159909

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868690T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706804T>C , CM000686.2:g.19706804T>C	GRCh38
NC_000024.9:g.21868690T>C , CM000686.1:g.21868690T>C	GRCh37
NC_000024.8:g.20328078T>C	NCBI36
NG_032920.1:g.43136A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.4059A>G MANE Select	ENSP00000322408.4:p.Gly1353=
ENST00000317961.8:c.4059A>G	ENSP00000322408.4:p.Gly1353=
ENST00000382806.6:c.3888A>G	ENSP00000372256.2:p.Gly1296=
ENST00000440077.5:c.3936A>G	ENSP00000398543.1:p.Gly1312=
ENST00000469599.6:n.2657A>G
ENST00000492117.1:n.3951A>G
ENST00000541639.5:c.4152A>G	ENSP00000444293.1:p.Gly1384=
NM_001146705.1:c.4152A>G	NP_001140177.1:p.Gly1384=
NM_001146706.1:c.3888A>G	NP_001140178.1:p.Gly1296=
NM_004653.4:c.4059A>G	NP_004644.2:p.Gly1353=
XM_005262560.1:c.3924A>G	XP_005262617.1:p.Gly1308=
XM_005262561.1:c.3828A>G	XP_005262618.1:p.Gly1276=
XM_011531468.1:c.3981A>G	XP_011529770.1:p.Gly1327=
XR_244571.2:n.4347A>G
XR_430568.2:n.4681A>G
XM_005262560.3:c.3924A>G	XP_005262617.1:p.Gly1308=
XM_005262561.3:c.3828A>G	XP_005262618.1:p.Gly1276=
XM_011531468.3:c.3981A>G	XP_011529770.1:p.Gly1327=
XM_024452495.1:c.2049A>G	XP_024308263.1:p.Gly683=
XM_024452496.1:c.1815A>G	XP_024308264.1:p.Gly605=
XR_001756009.2:n.4797A>G
XR_001756010.2:n.4797A>G
XR_001756011.2:n.4662A>G
XR_001756012.2:n.4810A>G
XR_001756013.2:n.4128A>G
XR_002958832.1:n.4229A>G
XR_002958834.1:n.4453A>G
XR_002958835.1:n.4336A>G
XR_002958836.1:n.5019A>G
XR_002958837.1:n.4826A>G
XR_244571.4:n.4346A>G
XR_430568.4:n.4680A>G
NM_001146706.2:c.3888A>G	NP_001140178.1:p.Gly1296=
NM_004653.5:c.4059A>G MANE Select	NP_004644.2:p.Gly1353=
NM_001146705.2:c.4152A>G	NP_001140177.1:p.Gly1384=