Canonical Allele Identifier: CA671773311
Gene: DIXDC1 HGNC NCBI

Linked Data

dbSNP Id: rs1253209106
MyVariant Identifiers: chr11:g.112016501C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112016501C>G , CM000673.2:g.112016501C>G GRCh38
NC_000011.9:g.111887225C>G , CM000673.1:g.111887225C>G GRCh37
NC_000011.8:g.111392435C>G NCBI36
NG_033127.1:g.94359C>G
NG_033127.2:g.94358C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000440460.7:c.1757-190C>G MANE Select ENSP00000394352.3:n.1757-190C>G
ENST00000440460.6:c.1757-190C>G ENSP00000394352.3:n.1757-190C>G
ENST00000526500.5:n.753-190C>G
ENST00000615255.1:c.1124-190C>G ENSP00000480808.1:n.1124-190C>G
ENST00000618522.4:n.1110-190C>G
NM_001037954.3:c.1757-190C>G NP_001033043.1:n.1757-190C>G
NM_033425.4:c.1124-190C>G NP_219493.1:n.1124-190C>G
XM_005277726.3:c.1757-190C>G XP_005277783.1:n.1757-190C>G
XM_005277727.3:c.1754-190C>G XP_005277784.1:n.1754-190C>G
XM_005277728.3:c.1124-190C>G XP_005277785.1:n.1124-190C>G
XM_011543045.1:c.875-190C>G XP_011541347.1:n.875-190C>G
XM_011543046.1:c.869-190C>G XP_011541348.1:n.869-190C>G
XM_017018466.2:c.1754-190C>G XP_016873955.1:n.1754-190C>G
XM_017018467.1:c.1754-190C>G XP_016873956.1:n.1754-190C>G
XM_017018468.1:c.875-190C>G XP_016873957.1:n.875-190C>G
XM_017018469.1:c.869-190C>G XP_016873958.1:n.869-190C>G
XM_024448742.1:c.1649-190C>G XP_024304510.1:n.1649-190C>G
XM_024448743.1:c.1646-190C>G XP_024304511.1:n.1646-190C>G
NM_001037954.4:c.1757-190C>G MANE Select NP_001033043.1:n.1757-190C>G
NM_033425.5:c.1124-190C>G NP_219493.1:n.1124-190C>G