Canonical Allele Identifier: CA671773710

Gene: DIXDC1

Linked Data

• dbSNP Id: rs1166474366
• gnomAD v3: 11-112016956-T-G
• gnomAD v4: 11-112016956-T-G
• MyVariant Identifiers: chr11:g.112016956T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112016956T>G , CM000673.2:g.112016956T>G	GRCh38
NC_000011.9:g.111887680T>G , CM000673.1:g.111887680T>G	GRCh37
NC_000011.8:g.111392890T>G	NCBI36
NG_033127.1:g.94814T>G
NG_033127.2:g.94813T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440460.7:c.1862+160T>G MANE Select	ENSP00000394352.3:n.1862+160T>G
ENST00000440460.6:c.1862+160T>G	ENSP00000394352.3:n.1862+160T>G
ENST00000526500.5:n.858+160T>G
ENST00000615255.1:c.1229+160T>G	ENSP00000480808.1:n.1229+160T>G
ENST00000618522.4:n.1215+160T>G
NM_001037954.3:c.1862+160T>G	NP_001033043.1:n.1862+160T>G
NM_033425.4:c.1229+160T>G	NP_219493.1:n.1229+160T>G
XM_005277726.3:c.1862+160T>G	XP_005277783.1:n.1862+160T>G
XM_005277727.3:c.1859+160T>G	XP_005277784.1:n.1859+160T>G
XM_005277728.3:c.1229+160T>G	XP_005277785.1:n.1229+160T>G
XM_011543045.1:c.980+160T>G	XP_011541347.1:n.980+160T>G
XM_011543046.1:c.974+160T>G	XP_011541348.1:n.974+160T>G
XM_017018466.2:c.1859+160T>G	XP_016873955.1:n.1859+160T>G
XM_017018467.1:c.1859+160T>G	XP_016873956.1:n.1859+160T>G
XM_017018468.1:c.980+160T>G	XP_016873957.1:n.980+160T>G
XM_017018469.1:c.974+160T>G	XP_016873958.1:n.974+160T>G
XM_024448742.1:c.1754+160T>G	XP_024304510.1:n.1754+160T>G
XM_024448743.1:c.1751+160T>G	XP_024304511.1:n.1751+160T>G
NM_001037954.4:c.1862+160T>G MANE Select	NP_001033043.1:n.1862+160T>G
NM_033425.5:c.1229+160T>G	NP_219493.1:n.1229+160T>G