Canonical Allele Identifier: CA2000523976
Gene: DIXDC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112016514A= , CM000673.2:g.112016514A= GRCh38
NC_000011.9:g.111887238A= , CM000673.1:g.111887238A= GRCh37
NC_000011.8:g.111392448A= NCBI36
NG_033127.1:g.94372A=
NG_033127.2:g.94371A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000440460.7:c.1757-177A= MANE Select ENSP00000394352.3:n.1757-177A=
ENST00000440460.6:c.1757-177A= ENSP00000394352.3:n.1757-177A=
ENST00000526500.5:n.753-177A=
ENST00000615255.1:c.1124-177A= ENSP00000480808.1:n.1124-177A=
ENST00000618522.4:n.1110-177A=
NM_001037954.3:c.1757-177A= NP_001033043.1:n.1757-177A=
NM_033425.4:c.1124-177A= NP_219493.1:n.1124-177A=
XM_005277726.3:c.1757-177A= XP_005277783.1:n.1757-177A=
XM_005277727.3:c.1754-177A= XP_005277784.1:n.1754-177A=
XM_005277728.3:c.1124-177A= XP_005277785.1:n.1124-177A=
XM_011543045.1:c.875-177A= XP_011541347.1:n.875-177A=
XM_011543046.1:c.869-177A= XP_011541348.1:n.869-177A=
XM_017018466.2:c.1754-177A= XP_016873955.1:n.1754-177A=
XM_017018467.1:c.1754-177A= XP_016873956.1:n.1754-177A=
XM_017018468.1:c.875-177A= XP_016873957.1:n.875-177A=
XM_017018469.1:c.869-177A= XP_016873958.1:n.869-177A=
XM_024448742.1:c.1649-177A= XP_024304510.1:n.1649-177A=
XM_024448743.1:c.1646-177A= XP_024304511.1:n.1646-177A=
NM_001037954.4:c.1757-177A= MANE Select NP_001033043.1:n.1757-177A=
NM_033425.5:c.1124-177A= NP_219493.1:n.1124-177A=