Canonical Allele Identifier: CA476785648
Gene: DIXDC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.111887512A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112016788A>T , CM000673.2:g.112016788A>T GRCh38
NC_000011.9:g.111887512A>T , CM000673.1:g.111887512A>T GRCh37
NC_000011.8:g.111392722A>T NCBI36
NG_033127.1:g.94646A>T
NG_033127.2:g.94645A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000440460.7:c.1854A>T MANE Select ENSP00000394352.3:p.Ile618=
ENST00000440460.6:c.1854A>T ENSP00000394352.3:p.Ile618=
ENST00000526500.5:n.850A>T
ENST00000615255.1:c.1221A>T ENSP00000480808.1:p.Ile407=
ENST00000618522.4:n.1207A>T
NM_001037954.3:c.1854A>T NP_001033043.1:p.Ile618=
NM_033425.4:c.1221A>T NP_219493.1:p.Ile407=
XM_005277726.3:c.1854A>T XP_005277783.1:p.Ile618=
XM_005277727.3:c.1851A>T XP_005277784.1:p.Ile617=
XM_005277728.3:c.1221A>T XP_005277785.1:p.Ile407=
XM_011543045.1:c.972A>T XP_011541347.1:p.Ile324=
XM_011543046.1:c.966A>T XP_011541348.1:p.Ile322=
XM_017018466.2:c.1851A>T XP_016873955.1:p.Ile617=
XM_017018467.1:c.1851A>T XP_016873956.1:p.Ile617=
XM_017018468.1:c.972A>T XP_016873957.1:p.Ile324=
XM_017018469.1:c.966A>T XP_016873958.1:p.Ile322=
XM_024448742.1:c.1746A>T XP_024304510.1:p.Ile582=
XM_024448743.1:c.1743A>T XP_024304511.1:p.Ile581=
NM_001037954.4:c.1854A>T MANE Select NP_001033043.1:p.Ile618=
NM_033425.5:c.1221A>T NP_219493.1:p.Ile407=