Canonical Allele Identifier: CA414843455

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869415A>C (hg19) ; chrY:g.19707529A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707529A>C , CM000686.2:g.19707529A>C	GRCh38
NC_000024.9:g.21869415A>C , CM000686.1:g.21869415A>C	GRCh37
NC_000024.8:g.20328803A>C	NCBI36
NG_032920.1:g.42411T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3617T>G MANE Select	ENSP00000322408.4:p.Leu1206Arg
ENST00000317961.8:c.3617T>G	ENSP00000322408.4:p.Leu1206Arg
ENST00000382806.6:c.3446T>G	ENSP00000372256.2:p.Leu1149Arg
ENST00000415360.1:c.533T>G	ENSP00000389433.1:p.Leu178Arg
ENST00000440077.5:c.3494T>G	ENSP00000398543.1:p.Leu1165Arg
ENST00000469599.6:n.2215T>G
ENST00000492117.1:n.3509T>G
ENST00000541639.5:c.3710T>G	ENSP00000444293.1:p.Leu1237Arg
NM_001146705.1:c.3710T>G	NP_001140177.1:p.Leu1237Arg
NM_001146706.1:c.3446T>G	NP_001140178.1:p.Leu1149Arg
NM_004653.4:c.3617T>G	NP_004644.2:p.Leu1206Arg
XM_005262560.1:c.3482T>G	XP_005262617.1:p.Leu1161Arg
XM_005262561.1:c.3386T>G	XP_005262618.1:p.Leu1129Arg
XM_011531468.1:c.3539T>G	XP_011529770.1:p.Leu1180Arg
XR_244571.2:n.3905T>G
XR_430568.2:n.4239T>G
XM_005262560.3:c.3482T>G	XP_005262617.1:p.Leu1161Arg
XM_005262561.3:c.3386T>G	XP_005262618.1:p.Leu1129Arg
XM_011531468.3:c.3539T>G	XP_011529770.1:p.Leu1180Arg
XM_024452495.1:c.1607T>G	XP_024308263.1:p.Leu536Arg
XM_024452496.1:c.1373T>G	XP_024308264.1:p.Leu458Arg
XR_001756009.2:n.4355T>G
XR_001756010.2:n.4355T>G
XR_001756011.2:n.4220T>G
XR_001756012.2:n.4368T>G
XR_001756013.2:n.3686T>G
XR_002958832.1:n.3787T>G
XR_002958834.1:n.4011T>G
XR_002958835.1:n.3894T>G
XR_002958836.1:n.4577T>G
XR_002958837.1:n.4384T>G
XR_244571.4:n.3904T>G
XR_430568.4:n.4238T>G
NM_001146706.2:c.3446T>G	NP_001140178.1:p.Leu1149Arg
NM_004653.5:c.3617T>G MANE Select	NP_004644.2:p.Leu1206Arg
NM_001146705.2:c.3710T>G	NP_001140177.1:p.Leu1237Arg