Canonical Allele Identifier: CA520160805

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869826G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707940G>C , CM000686.2:g.19707940G>C	GRCh38
NC_000024.9:g.21869826G>C , CM000686.1:g.21869826G>C	GRCh37
NC_000024.8:g.20329214G>C	NCBI36
NG_032920.1:g.42000C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.3393C>G MANE Select	ENSP00000322408.4:p.Gly1131=
ENST00000317961.8:c.3393C>G	ENSP00000322408.4:p.Gly1131=
ENST00000382806.6:c.3222C>G	ENSP00000372256.2:p.Gly1074=
ENST00000415360.1:c.309C>G	ENSP00000389433.1:p.Gly103=
ENST00000440077.5:c.3270C>G	ENSP00000398543.1:p.Gly1090=
ENST00000469599.6:n.1991C>G
ENST00000492117.1:n.3285C>G
ENST00000541639.5:c.3486C>G	ENSP00000444293.1:p.Gly1162=
NM_001146705.1:c.3486C>G	NP_001140177.1:p.Gly1162=
NM_001146706.1:c.3222C>G	NP_001140178.1:p.Gly1074=
NM_004653.4:c.3393C>G	NP_004644.2:p.Gly1131=
XM_005262560.1:c.3258C>G	XP_005262617.1:p.Gly1086=
XM_005262561.1:c.3162C>G	XP_005262618.1:p.Gly1054=
XM_011531468.1:c.3315C>G	XP_011529770.1:p.Gly1105=
XR_244571.2:n.3681C>G
XR_430568.2:n.4015C>G
XM_005262560.3:c.3258C>G	XP_005262617.1:p.Gly1086=
XM_005262561.3:c.3162C>G	XP_005262618.1:p.Gly1054=
XM_011531468.3:c.3315C>G	XP_011529770.1:p.Gly1105=
XM_024452495.1:c.1383C>G	XP_024308263.1:p.Gly461=
XM_024452496.1:c.1149C>G	XP_024308264.1:p.Gly383=
XR_001756009.2:n.4131C>G
XR_001756010.2:n.4131C>G
XR_001756011.2:n.3996C>G
XR_001756012.2:n.4144C>G
XR_001756013.2:n.3462C>G
XR_002958832.1:n.3563C>G
XR_002958834.1:n.3787C>G
XR_002958835.1:n.3670C>G
XR_002958836.1:n.4353C>G
XR_002958837.1:n.4160C>G
XR_244571.4:n.3680C>G
XR_430568.4:n.4014C>G
NM_001146706.2:c.3222C>G	NP_001140178.1:p.Gly1074=
NM_004653.5:c.3393C>G MANE Select	NP_004644.2:p.Gly1131=
NM_001146705.2:c.3486C>G	NP_001140177.1:p.Gly1162=