Canonical Allele Identifier: CA2000523999
Gene: DIXDC1 HGNC NCBI

Linked Data

dbSNP Id: rs1861597558

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112016574_112016575del , CM000673.2:g.112016574_112016575del GRCh38
NC_000011.9:g.111887298_111887299del , CM000673.1:g.111887298_111887299del GRCh37
NC_000011.8:g.111392508_111392509del NCBI36
NG_033127.1:g.94432_94433del
NG_033127.2:g.94431_94432del

Transcript Alleles

HGVS Amino-acid Change
ENST00000440460.7:c.1757-117_1757-116del MANE Select ENSP00000394352.3:n.1757-117_1757-116del
ENST00000440460.6:c.1757-117_1757-116del ENSP00000394352.3:n.1757-117_1757-116del
ENST00000526500.5:n.753-117_753-116del
ENST00000615255.1:c.1124-117_1124-116del ENSP00000480808.1:n.1124-117_1124-116del
ENST00000618522.4:n.1110-117_1110-116del
NM_001037954.3:c.1757-117_1757-116del NP_001033043.1:n.1757-117_1757-116del
NM_033425.4:c.1124-117_1124-116del NP_219493.1:n.1124-117_1124-116del
XM_005277726.3:c.1757-117_1757-116del XP_005277783.1:n.1757-117_1757-116del
XM_005277727.3:c.1754-117_1754-116del XP_005277784.1:n.1754-117_1754-116del
XM_005277728.3:c.1124-117_1124-116del XP_005277785.1:n.1124-117_1124-116del
XM_011543045.1:c.875-117_875-116del XP_011541347.1:n.875-117_875-116del
XM_011543046.1:c.869-117_869-116del XP_011541348.1:n.869-117_869-116del
XM_017018466.2:c.1754-117_1754-116del XP_016873955.1:n.1754-117_1754-116del
XM_017018467.1:c.1754-117_1754-116del XP_016873956.1:n.1754-117_1754-116del
XM_017018468.1:c.875-117_875-116del XP_016873957.1:n.875-117_875-116del
XM_017018469.1:c.869-117_869-116del XP_016873958.1:n.869-117_869-116del
XM_024448742.1:c.1649-117_1649-116del XP_024304510.1:n.1649-117_1649-116del
XM_024448743.1:c.1646-117_1646-116del XP_024304511.1:n.1646-117_1646-116del
NM_001037954.4:c.1757-117_1757-116del MANE Select NP_001033043.1:n.1757-117_1757-116del
NM_033425.5:c.1124-117_1124-116del NP_219493.1:n.1124-117_1124-116del