Canonical Allele Identifier: CA2000524086
Gene: DIXDC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112016842A= , CM000673.2:g.112016842A= GRCh38
NC_000011.9:g.111887566A= , CM000673.1:g.111887566A= GRCh37
NC_000011.8:g.111392776A= NCBI36
NG_033127.1:g.94700A=
NG_033127.2:g.94699A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000440460.7:c.1862+46A= MANE Select ENSP00000394352.3:n.1862+46A=
ENST00000440460.6:c.1862+46A= ENSP00000394352.3:n.1862+46A=
ENST00000526500.5:n.858+46A=
ENST00000615255.1:c.1229+46A= ENSP00000480808.1:n.1229+46A=
ENST00000618522.4:n.1215+46A=
NM_001037954.3:c.1862+46A= NP_001033043.1:n.1862+46A=
NM_033425.4:c.1229+46A= NP_219493.1:n.1229+46A=
XM_005277726.3:c.1862+46A= XP_005277783.1:n.1862+46A=
XM_005277727.3:c.1859+46A= XP_005277784.1:n.1859+46A=
XM_005277728.3:c.1229+46A= XP_005277785.1:n.1229+46A=
XM_011543045.1:c.980+46A= XP_011541347.1:n.980+46A=
XM_011543046.1:c.974+46A= XP_011541348.1:n.974+46A=
XM_017018466.2:c.1859+46A= XP_016873955.1:n.1859+46A=
XM_017018467.1:c.1859+46A= XP_016873956.1:n.1859+46A=
XM_017018468.1:c.980+46A= XP_016873957.1:n.980+46A=
XM_017018469.1:c.974+46A= XP_016873958.1:n.974+46A=
XM_024448742.1:c.1754+46A= XP_024304510.1:n.1754+46A=
XM_024448743.1:c.1751+46A= XP_024304511.1:n.1751+46A=
NM_001037954.4:c.1862+46A= MANE Select NP_001033043.1:n.1862+46A=
NM_033425.5:c.1229+46A= NP_219493.1:n.1229+46A=