Canonical Allele Identifier: CA2000511843
Gene: DIXDC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111989050A= , CM000673.2:g.111989050A= GRCh38
NC_000011.9:g.111859774A= , CM000673.1:g.111859774A= GRCh37
NC_000011.8:g.111364984A= NCBI36
NG_033127.1:g.66908A=
NG_033127.2:g.66907A=

Transcript Alleles

HGVS Amino-acid Change
NM_001037954.4:c.1108A= MANE Select NP_001033043.1:p.Ile370=
ENST00000440460.7:c.1108A= MANE Select ENSP00000394352.3:p.Ile370=
NM_001037954.3:c.1108A= NP_001033043.1:p.Ile370=
NM_033425.4:c.475A= NP_219493.1:p.Ile159=
NM_033425.5:c.475A= NP_219493.1:p.Ile159=
ENST00000440460.6:c.1108A= ENSP00000394352.3:p.Ile370=
ENST00000526500.5:n.104A=
ENST00000614104.4:c.226A= ENSP00000479434.1:p.Ile76=
ENST00000615255.1:c.475A= ENSP00000480808.1:p.Ile159=
ENST00000618522.4:n.461A=
XM_005277726.3:c.1108A= XP_005277783.1:p.Ile370=
XM_005277727.3:c.1105A= XP_005277784.1:p.Ile369=
XM_005277728.3:c.475A= XP_005277785.1:p.Ile159=
XM_011543045.1:c.226A= XP_011541347.1:p.Ile76=
XM_011543046.1:c.220A= XP_011541348.1:p.Ile74=
XM_017018466.2:c.1105A= XP_016873955.1:p.Ile369=
XM_017018467.1:c.1105A= XP_016873956.1:p.Ile369=
XM_017018468.1:c.226A= XP_016873957.1:p.Ile76=
XM_017018469.1:c.220A= XP_016873958.1:p.Ile74=
XM_024448742.1:c.1000A= XP_024304510.1:p.Ile334=
XM_024448743.1:c.997A= XP_024304511.1:p.Ile333=