Canonical Allele Identifier: CA520159277
Gene: KDM5D HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21867928A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19706042A>G , CM000686.2:g.19706042A>G GRCh38
NC_000024.9:g.21867928A>G , CM000686.1:g.21867928A>G GRCh37
NC_000024.8:g.20327316A>G NCBI36
NG_032920.1:g.43898T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.4573T>C MANE Select ENSP00000322408.4:p.Leu1525=
ENST00000317961.8:c.4573T>C ENSP00000322408.4:p.Leu1525=
ENST00000382806.6:c.4402T>C ENSP00000372256.2:p.Leu1468=
ENST00000469599.6:n.3324T>C
ENST00000492117.1:n.4618T>C
ENST00000541639.5:c.4666T>C ENSP00000444293.1:p.Leu1556=
NM_001146705.1:c.4666T>C NP_001140177.1:p.Leu1556=
NM_001146706.1:c.4402T>C NP_001140178.1:p.Leu1468=
NM_004653.4:c.4573T>C NP_004644.2:p.Leu1525=
XM_005262560.1:c.4438T>C XP_005262617.1:p.Leu1480=
XM_005262561.1:c.4342T>C XP_005262618.1:p.Leu1448=
XM_011531468.1:c.4495T>C XP_011529770.1:p.Leu1499=
XR_430568.2:n.5348T>C
XM_005262560.3:c.4438T>C XP_005262617.1:p.Leu1480=
XM_005262561.3:c.4342T>C XP_005262618.1:p.Leu1448=
XM_011531468.3:c.4495T>C XP_011529770.1:p.Leu1499=
XM_024452495.1:c.2563T>C XP_024308263.1:p.Leu855=
XM_024452496.1:c.2329T>C XP_024308264.1:p.Leu777=
XR_001756009.2:n.5311T>C
XR_001756010.2:n.5279T>C
XR_001756011.2:n.5176T>C
XR_001756012.2:n.5324T>C
XR_001756013.2:n.4642T>C
XR_002958832.1:n.4896T>C
XR_002958834.1:n.4967T>C
XR_002958835.1:n.4850T>C
XR_002958836.1:n.5501T>C
XR_002958837.1:n.5308T>C
XR_244571.4:n.4828T>C
XR_430568.4:n.5347T>C
NM_001146706.2:c.4402T>C NP_001140178.1:p.Leu1468=
NM_004653.5:c.4573T>C MANE Select NP_004644.2:p.Leu1525=
NM_001146705.2:c.4666T>C NP_001140177.1:p.Leu1556=