Canonical Allele Identifier: CA337440091
Gene: KDM5D HGNC NCBI

Linked Data

dbSNP Id: rs2032641

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19711401C>T , CM000686.2:g.19711401C>T GRCh38
NC_000024.9:g.21873287C>T , CM000686.1:g.21873287C>T GRCh37
NC_000024.8:g.20332675C>T NCBI36
NG_032920.1:g.38539G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317961.9:c.2487-929G>A MANE Select ENSP00000322408.4:n.2487-929G>A
ENST00000317961.8:c.2487-929G>A ENSP00000322408.4:n.2487-929G>A
ENST00000382806.6:c.2316-929G>A ENSP00000372256.2:n.2316-929G>A
ENST00000440077.5:c.2364-929G>A ENSP00000398543.1:n.2364-929G>A
ENST00000469599.6:n.634-929G>A
ENST00000492117.1:n.2379-929G>A
ENST00000541639.5:c.2580-929G>A ENSP00000444293.1:n.2580-929G>A
NM_001146705.1:c.2580-929G>A NP_001140177.1:n.2580-929G>A
NM_001146706.1:c.2316-929G>A NP_001140178.1:n.2316-929G>A
NM_004653.4:c.2487-929G>A NP_004644.2:n.2487-929G>A
XM_005262560.1:c.2352-929G>A XP_005262617.1:n.2352-929G>A
XM_005262561.1:c.2487-929G>A XP_005262618.1:n.2487-929G>A
XM_005262562.2:c.2487-929G>A XP_005262619.1:n.2487-929G>A
XM_011531468.1:c.2487-929G>A XP_011529770.1:n.2487-929G>A
XR_244571.2:n.2775-929G>A
XR_430568.2:n.2658-929G>A
XR_938609.1:n.2627-929G>A
XR_938610.1:n.2627-929G>A
XM_005262560.3:c.2352-929G>A XP_005262617.1:n.2352-929G>A
XM_005262561.3:c.2487-929G>A XP_005262618.1:n.2487-929G>A
XM_011531468.3:c.2487-929G>A XP_011529770.1:n.2487-929G>A
XM_024452495.1:c.477-929G>A XP_024308263.1:n.477-929G>A
XM_024452496.1:c.243-929G>A XP_024308264.1:n.243-929G>A
XR_001756009.2:n.2774-929G>A
XR_001756010.2:n.2774-929G>A
XR_001756011.2:n.2639-929G>A
XR_001756012.2:n.2787-929G>A
XR_001756013.2:n.2787-929G>A
XR_002958832.1:n.2657-929G>A
XR_002958833.1:n.2787-929G>A
XR_002958834.1:n.2881-929G>A
XR_002958835.1:n.2764-929G>A
XR_002958836.1:n.2881-929G>A
XR_002958837.1:n.2881-929G>A
XR_244571.4:n.2774-929G>A
XR_430568.4:n.2657-929G>A
NM_001146706.2:c.2316-929G>A NP_001140178.1:n.2316-929G>A
NM_004653.5:c.2487-929G>A MANE Select NP_004644.2:n.2487-929G>A
NM_001146705.2:c.2580-929G>A NP_001140177.1:n.2580-929G>A