Canonical Allele Identifier: CA414844479

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869891G>C (hg19) ; chrY:g.19708005G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708005G>C , CM000686.2:g.19708005G>C	GRCh38
NC_000024.9:g.21869891G>C , CM000686.1:g.21869891G>C	GRCh37
NC_000024.8:g.20329279G>C	NCBI36
NG_032920.1:g.41935C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3328C>G MANE Select	ENSP00000322408.4:p.Leu1110Val
ENST00000317961.8:c.3328C>G	ENSP00000322408.4:p.Leu1110Val
ENST00000382806.6:c.3157C>G	ENSP00000372256.2:p.Leu1053Val
ENST00000415360.1:c.244C>G	ENSP00000389433.1:p.Leu82Val
ENST00000440077.5:c.3205C>G	ENSP00000398543.1:p.Leu1069Val
ENST00000469599.6:n.1926C>G
ENST00000492117.1:n.3220C>G
ENST00000541639.5:c.3421C>G	ENSP00000444293.1:p.Leu1141Val
NM_001146705.1:c.3421C>G	NP_001140177.1:p.Leu1141Val
NM_001146706.1:c.3157C>G	NP_001140178.1:p.Leu1053Val
NM_004653.4:c.3328C>G	NP_004644.2:p.Leu1110Val
XM_005262560.1:c.3193C>G	XP_005262617.1:p.Leu1065Val
XM_005262561.1:c.3097C>G	XP_005262618.1:p.Leu1033Val
XM_011531468.1:c.3250C>G	XP_011529770.1:p.Leu1084Val
XR_244571.2:n.3616C>G
XR_430568.2:n.3950C>G
XM_005262560.3:c.3193C>G	XP_005262617.1:p.Leu1065Val
XM_005262561.3:c.3097C>G	XP_005262618.1:p.Leu1033Val
XM_011531468.3:c.3250C>G	XP_011529770.1:p.Leu1084Val
XM_024452495.1:c.1318C>G	XP_024308263.1:p.Leu440Val
XM_024452496.1:c.1084C>G	XP_024308264.1:p.Leu362Val
XR_001756009.2:n.4066C>G
XR_001756010.2:n.4066C>G
XR_001756011.2:n.3931C>G
XR_001756012.2:n.4079C>G
XR_001756013.2:n.3397C>G
XR_002958832.1:n.3498C>G
XR_002958834.1:n.3722C>G
XR_002958835.1:n.3605C>G
XR_002958836.1:n.4288C>G
XR_002958837.1:n.4095C>G
XR_244571.4:n.3615C>G
XR_430568.4:n.3949C>G
NM_001146706.2:c.3157C>G	NP_001140178.1:p.Leu1053Val
NM_004653.5:c.3328C>G MANE Select	NP_004644.2:p.Leu1110Val
NM_001146705.2:c.3421C>G	NP_001140177.1:p.Leu1141Val