Canonical Allele Identifier: CA382590399

Gene: DIXDC1

Linked Data

• MyVariant Identifiers: chr11:g.111887498T>A (hg19) ; chr11:g.112016774T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112016774T>A , CM000673.2:g.112016774T>A	GRCh38
NC_000011.9:g.111887498T>A , CM000673.1:g.111887498T>A	GRCh37
NC_000011.8:g.111392708T>A	NCBI36
NG_033127.1:g.94632T>A
NG_033127.2:g.94631T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000440460.7:c.1840T>A MANE Select	ENSP00000394352.3:p.Phe614Ile
ENST00000440460.6:c.1840T>A	ENSP00000394352.3:p.Phe614Ile
ENST00000526500.5:n.836T>A
ENST00000615255.1:c.1207T>A	ENSP00000480808.1:p.Phe403Ile
ENST00000618522.4:n.1193T>A
NM_001037954.3:c.1840T>A	NP_001033043.1:p.Phe614Ile
NM_033425.4:c.1207T>A	NP_219493.1:p.Phe403Ile
XM_005277726.3:c.1840T>A	XP_005277783.1:p.Phe614Ile
XM_005277727.3:c.1837T>A	XP_005277784.1:p.Phe613Ile
XM_005277728.3:c.1207T>A	XP_005277785.1:p.Phe403Ile
XM_011543045.1:c.958T>A	XP_011541347.1:p.Phe320Ile
XM_011543046.1:c.952T>A	XP_011541348.1:p.Phe318Ile
XM_017018466.2:c.1837T>A	XP_016873955.1:p.Phe613Ile
XM_017018467.1:c.1837T>A	XP_016873956.1:p.Phe613Ile
XM_017018468.1:c.958T>A	XP_016873957.1:p.Phe320Ile
XM_017018469.1:c.952T>A	XP_016873958.1:p.Phe318Ile
XM_024448742.1:c.1732T>A	XP_024304510.1:p.Phe578Ile
XM_024448743.1:c.1729T>A	XP_024304511.1:p.Phe577Ile
NM_001037954.4:c.1840T>A MANE Select	NP_001033043.1:p.Phe614Ile
NM_033425.5:c.1207T>A	NP_219493.1:p.Phe403Ile