Canonical Allele Identifier: CA15870458

Gene: DBNDD1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.90018153C>T , CM000678.2:g.90018153C>T	GRCh38
NC_000016.9:g.90084561C>T , CM000678.1:g.90084561C>T	GRCh37
NC_000016.8:g.88612062C>T	NCBI36
NG_046598.1:g.3525C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000002501.11:c.31+1158G>A MANE Select	ENSP00000002501.6:n.31+1158G>A
ENST00000568838.2:c.-216+1575G>A	ENSP00000457625.2:n.-216+1575G>A
ENST00000002501.10:c.31+1158G>A	ENSP00000002501.6:n.31+1158G>A
ENST00000568330.2:c.153+1575G>A
ENST00000568838.1:c.391+1575G>A	ENSP00000457625.1:n.391+1575G>A
NM_001042610.2:c.31+1158G>A	NP_001036075.1:n.31+1158G>A
NM_001288708.1:c.-83+1575G>A	NP_001275637.1:n.-83+1575G>A
NM_001288709.1:c.391+1575G>A	NP_001275638.1:n.391+1575G>A
NM_001042610.3:c.31+1158G>A MANE Select	NP_001036075.1:n.31+1158G>A
NM_001288708.2:c.-83+1575G>A	NP_001275637.1:n.-83+1575G>A
NM_001288709.2:c.-216+1575G>A	NP_001275638.2:n.-216+1575G>A