Canonical Allele Identifier: CA414844463

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869887C>A (hg19) ; chrY:g.19708001C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708001C>A , CM000686.2:g.19708001C>A	GRCh38
NC_000024.9:g.21869887C>A , CM000686.1:g.21869887C>A	GRCh37
NC_000024.8:g.20329275C>A	NCBI36
NG_032920.1:g.41939G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3332G>T MANE Select	ENSP00000322408.4:p.Gly1111Val
ENST00000317961.8:c.3332G>T	ENSP00000322408.4:p.Gly1111Val
ENST00000382806.6:c.3161G>T	ENSP00000372256.2:p.Gly1054Val
ENST00000415360.1:c.248G>T	ENSP00000389433.1:p.Gly83Val
ENST00000440077.5:c.3209G>T	ENSP00000398543.1:p.Gly1070Val
ENST00000469599.6:n.1930G>T
ENST00000492117.1:n.3224G>T
ENST00000541639.5:c.3425G>T	ENSP00000444293.1:p.Gly1142Val
NM_001146705.1:c.3425G>T	NP_001140177.1:p.Gly1142Val
NM_001146706.1:c.3161G>T	NP_001140178.1:p.Gly1054Val
NM_004653.4:c.3332G>T	NP_004644.2:p.Gly1111Val
XM_005262560.1:c.3197G>T	XP_005262617.1:p.Gly1066Val
XM_005262561.1:c.3101G>T	XP_005262618.1:p.Gly1034Val
XM_011531468.1:c.3254G>T	XP_011529770.1:p.Gly1085Val
XR_244571.2:n.3620G>T
XR_430568.2:n.3954G>T
XM_005262560.3:c.3197G>T	XP_005262617.1:p.Gly1066Val
XM_005262561.3:c.3101G>T	XP_005262618.1:p.Gly1034Val
XM_011531468.3:c.3254G>T	XP_011529770.1:p.Gly1085Val
XM_024452495.1:c.1322G>T	XP_024308263.1:p.Gly441Val
XM_024452496.1:c.1088G>T	XP_024308264.1:p.Gly363Val
XR_001756009.2:n.4070G>T
XR_001756010.2:n.4070G>T
XR_001756011.2:n.3935G>T
XR_001756012.2:n.4083G>T
XR_001756013.2:n.3401G>T
XR_002958832.1:n.3502G>T
XR_002958834.1:n.3726G>T
XR_002958835.1:n.3609G>T
XR_002958836.1:n.4292G>T
XR_002958837.1:n.4099G>T
XR_244571.4:n.3619G>T
XR_430568.4:n.3953G>T
NM_001146706.2:c.3161G>T	NP_001140178.1:p.Gly1054Val
NM_004653.5:c.3332G>T MANE Select	NP_004644.2:p.Gly1111Val
NM_001146705.2:c.3425G>T	NP_001140177.1:p.Gly1142Val