Canonical Allele Identifier: CA414843176

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869335G>C (hg19) ; chrY:g.19707449G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707449G>C , CM000686.2:g.19707449G>C	GRCh38
NC_000024.9:g.21869335G>C , CM000686.1:g.21869335G>C	GRCh37
NC_000024.8:g.20328723G>C	NCBI36
NG_032920.1:g.42491C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3697C>G MANE Select	ENSP00000322408.4:p.Leu1233Val
ENST00000317961.8:c.3697C>G	ENSP00000322408.4:p.Leu1233Val
ENST00000382806.6:c.3526C>G	ENSP00000372256.2:p.Leu1176Val
ENST00000415360.1:c.613C>G	ENSP00000389433.1:p.Leu205Val
ENST00000440077.5:c.3574C>G	ENSP00000398543.1:p.Leu1192Val
ENST00000469599.6:n.2295C>G
ENST00000492117.1:n.3589C>G
ENST00000541639.5:c.3790C>G	ENSP00000444293.1:p.Leu1264Val
NM_001146705.1:c.3790C>G	NP_001140177.1:p.Leu1264Val
NM_001146706.1:c.3526C>G	NP_001140178.1:p.Leu1176Val
NM_004653.4:c.3697C>G	NP_004644.2:p.Leu1233Val
XM_005262560.1:c.3562C>G	XP_005262617.1:p.Leu1188Val
XM_005262561.1:c.3466C>G	XP_005262618.1:p.Leu1156Val
XM_011531468.1:c.3619C>G	XP_011529770.1:p.Leu1207Val
XR_244571.2:n.3985C>G
XR_430568.2:n.4319C>G
XM_005262560.3:c.3562C>G	XP_005262617.1:p.Leu1188Val
XM_005262561.3:c.3466C>G	XP_005262618.1:p.Leu1156Val
XM_011531468.3:c.3619C>G	XP_011529770.1:p.Leu1207Val
XM_024452495.1:c.1687C>G	XP_024308263.1:p.Leu563Val
XM_024452496.1:c.1453C>G	XP_024308264.1:p.Leu485Val
XR_001756009.2:n.4435C>G
XR_001756010.2:n.4435C>G
XR_001756011.2:n.4300C>G
XR_001756012.2:n.4448C>G
XR_001756013.2:n.3766C>G
XR_002958832.1:n.3867C>G
XR_002958834.1:n.4091C>G
XR_002958835.1:n.3974C>G
XR_002958836.1:n.4657C>G
XR_002958837.1:n.4464C>G
XR_244571.4:n.3984C>G
XR_430568.4:n.4318C>G
NM_001146706.2:c.3526C>G	NP_001140178.1:p.Leu1176Val
NM_004653.5:c.3697C>G MANE Select	NP_004644.2:p.Leu1233Val
NM_001146705.2:c.3790C>G	NP_001140177.1:p.Leu1264Val