Canonical Allele Identifier: CA476785550

Gene: DIXDC1

Linked Data

• MyVariant Identifiers: chr11:g.111887422T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112016698T>G , CM000673.2:g.112016698T>G	GRCh38
NC_000011.9:g.111887422T>G , CM000673.1:g.111887422T>G	GRCh37
NC_000011.8:g.111392632T>G	NCBI36
NG_033127.1:g.94556T>G
NG_033127.2:g.94555T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440460.7:c.1764T>G MANE Select	ENSP00000394352.3:p.Pro588=
ENST00000440460.6:c.1764T>G	ENSP00000394352.3:p.Pro588=
ENST00000526500.5:n.760T>G
ENST00000615255.1:c.1131T>G	ENSP00000480808.1:p.Pro377=
ENST00000618522.4:n.1117T>G
NM_001037954.3:c.1764T>G	NP_001033043.1:p.Pro588=
NM_033425.4:c.1131T>G	NP_219493.1:p.Pro377=
XM_005277726.3:c.1764T>G	XP_005277783.1:p.Pro588=
XM_005277727.3:c.1761T>G	XP_005277784.1:p.Pro587=
XM_005277728.3:c.1131T>G	XP_005277785.1:p.Pro377=
XM_011543045.1:c.882T>G	XP_011541347.1:p.Pro294=
XM_011543046.1:c.876T>G	XP_011541348.1:p.Pro292=
XM_017018466.2:c.1761T>G	XP_016873955.1:p.Pro587=
XM_017018467.1:c.1761T>G	XP_016873956.1:p.Pro587=
XM_017018468.1:c.882T>G	XP_016873957.1:p.Pro294=
XM_017018469.1:c.876T>G	XP_016873958.1:p.Pro292=
XM_024448742.1:c.1656T>G	XP_024304510.1:p.Pro552=
XM_024448743.1:c.1653T>G	XP_024304511.1:p.Pro551=
NM_001037954.4:c.1764T>G MANE Select	NP_001033043.1:p.Pro588=
NM_033425.5:c.1131T>G	NP_219493.1:p.Pro377=