Canonical Allele Identifier: CA414844375

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869864G>T (hg19) ; chrY:g.19707978G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707978G>T , CM000686.2:g.19707978G>T	GRCh38
NC_000024.9:g.21869864G>T , CM000686.1:g.21869864G>T	GRCh37
NC_000024.8:g.20329252G>T	NCBI36
NG_032920.1:g.41962C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3355C>A MANE Select	ENSP00000322408.4:p.Leu1119Met
ENST00000317961.8:c.3355C>A	ENSP00000322408.4:p.Leu1119Met
ENST00000382806.6:c.3184C>A	ENSP00000372256.2:p.Leu1062Met
ENST00000415360.1:c.271C>A	ENSP00000389433.1:p.Leu91Met
ENST00000440077.5:c.3232C>A	ENSP00000398543.1:p.Leu1078Met
ENST00000469599.6:n.1953C>A
ENST00000492117.1:n.3247C>A
ENST00000541639.5:c.3448C>A	ENSP00000444293.1:p.Leu1150Met
NM_001146705.1:c.3448C>A	NP_001140177.1:p.Leu1150Met
NM_001146706.1:c.3184C>A	NP_001140178.1:p.Leu1062Met
NM_004653.4:c.3355C>A	NP_004644.2:p.Leu1119Met
XM_005262560.1:c.3220C>A	XP_005262617.1:p.Leu1074Met
XM_005262561.1:c.3124C>A	XP_005262618.1:p.Leu1042Met
XM_011531468.1:c.3277C>A	XP_011529770.1:p.Leu1093Met
XR_244571.2:n.3643C>A
XR_430568.2:n.3977C>A
XM_005262560.3:c.3220C>A	XP_005262617.1:p.Leu1074Met
XM_005262561.3:c.3124C>A	XP_005262618.1:p.Leu1042Met
XM_011531468.3:c.3277C>A	XP_011529770.1:p.Leu1093Met
XM_024452495.1:c.1345C>A	XP_024308263.1:p.Leu449Met
XM_024452496.1:c.1111C>A	XP_024308264.1:p.Leu371Met
XR_001756009.2:n.4093C>A
XR_001756010.2:n.4093C>A
XR_001756011.2:n.3958C>A
XR_001756012.2:n.4106C>A
XR_001756013.2:n.3424C>A
XR_002958832.1:n.3525C>A
XR_002958834.1:n.3749C>A
XR_002958835.1:n.3632C>A
XR_002958836.1:n.4315C>A
XR_002958837.1:n.4122C>A
XR_244571.4:n.3642C>A
XR_430568.4:n.3976C>A
NM_001146706.2:c.3184C>A	NP_001140178.1:p.Leu1062Met
NM_004653.5:c.3355C>A MANE Select	NP_004644.2:p.Leu1119Met
NM_001146705.2:c.3448C>A	NP_001140177.1:p.Leu1150Met