Canonical Allele Identifier: CA382589846
Gene: DIXDC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112016697C>A , CM000673.2:g.112016697C>A GRCh38
NC_000011.9:g.111887421C>A , CM000673.1:g.111887421C>A GRCh37
NC_000011.8:g.111392631C>A NCBI36
NG_033127.1:g.94555C>A
NG_033127.2:g.94554C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000440460.7:c.1763C>A MANE Select ENSP00000394352.3:p.Pro588His
ENST00000440460.6:c.1763C>A ENSP00000394352.3:p.Pro588His
ENST00000526500.5:n.759C>A
ENST00000615255.1:c.1130C>A ENSP00000480808.1:p.Pro377His
ENST00000618522.4:n.1116C>A
NM_001037954.3:c.1763C>A NP_001033043.1:p.Pro588His
NM_033425.4:c.1130C>A NP_219493.1:p.Pro377His
XM_005277726.3:c.1763C>A XP_005277783.1:p.Pro588His
XM_005277727.3:c.1760C>A XP_005277784.1:p.Pro587His
XM_005277728.3:c.1130C>A XP_005277785.1:p.Pro377His
XM_011543045.1:c.881C>A XP_011541347.1:p.Pro294His
XM_011543046.1:c.875C>A XP_011541348.1:p.Pro292His
XM_017018466.2:c.1760C>A XP_016873955.1:p.Pro587His
XM_017018467.1:c.1760C>A XP_016873956.1:p.Pro587His
XM_017018468.1:c.881C>A XP_016873957.1:p.Pro294His
XM_017018469.1:c.875C>A XP_016873958.1:p.Pro292His
XM_024448742.1:c.1655C>A XP_024304510.1:p.Pro552His
XM_024448743.1:c.1652C>A XP_024304511.1:p.Pro551His
NM_001037954.4:c.1763C>A MANE Select NP_001033043.1:p.Pro588His
NM_033425.5:c.1130C>A NP_219493.1:p.Pro377His