Canonical Allele Identifier: CA414841932
Gene: KDM5D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19706815T>G , CM000686.2:g.19706815T>G GRCh38
NC_000024.9:g.21868701T>G , CM000686.1:g.21868701T>G GRCh37
NC_000024.8:g.20328089T>G NCBI36
NG_032920.1:g.43125A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.4048A>C MANE Select ENSP00000322408.4:p.Met1350Leu
ENST00000317961.8:c.4048A>C ENSP00000322408.4:p.Met1350Leu
ENST00000382806.6:c.3877A>C ENSP00000372256.2:p.Met1293Leu
ENST00000440077.5:c.3925A>C ENSP00000398543.1:p.Met1309Leu
ENST00000469599.6:n.2646A>C
ENST00000492117.1:n.3940A>C
ENST00000541639.5:c.4141A>C ENSP00000444293.1:p.Met1381Leu
NM_001146705.1:c.4141A>C NP_001140177.1:p.Met1381Leu
NM_001146706.1:c.3877A>C NP_001140178.1:p.Met1293Leu
NM_004653.4:c.4048A>C NP_004644.2:p.Met1350Leu
XM_005262560.1:c.3913A>C XP_005262617.1:p.Met1305Leu
XM_005262561.1:c.3817A>C XP_005262618.1:p.Met1273Leu
XM_011531468.1:c.3970A>C XP_011529770.1:p.Met1324Leu
XR_244571.2:n.4336A>C
XR_430568.2:n.4670A>C
XM_005262560.3:c.3913A>C XP_005262617.1:p.Met1305Leu
XM_005262561.3:c.3817A>C XP_005262618.1:p.Met1273Leu
XM_011531468.3:c.3970A>C XP_011529770.1:p.Met1324Leu
XM_024452495.1:c.2038A>C XP_024308263.1:p.Met680Leu
XM_024452496.1:c.1804A>C XP_024308264.1:p.Met602Leu
XR_001756009.2:n.4786A>C
XR_001756010.2:n.4786A>C
XR_001756011.2:n.4651A>C
XR_001756012.2:n.4799A>C
XR_001756013.2:n.4117A>C
XR_002958832.1:n.4218A>C
XR_002958834.1:n.4442A>C
XR_002958835.1:n.4325A>C
XR_002958836.1:n.5008A>C
XR_002958837.1:n.4815A>C
XR_244571.4:n.4335A>C
XR_430568.4:n.4669A>C
NM_001146706.2:c.3877A>C NP_001140178.1:p.Met1293Leu
NM_004653.5:c.4048A>C MANE Select NP_004644.2:p.Met1350Leu
NM_001146705.2:c.4141A>C NP_001140177.1:p.Met1381Leu