Canonical Allele Identifier: CA886051406

Gene: VTCN1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117210906G>T , CM000663.2:g.117210906G>T	GRCh38
NC_000001.10:g.117753528G>T , CM000663.1:g.117753528G>T	GRCh37
NC_000001.9:g.117555051G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.-51C>A MANE Select	ENSP00000358470.3:n.-51C>A
ENST00000328189.7:c.-51C>A	ENSP00000328168.3:n.-51C>A
ENST00000369458.7:c.-51C>A	ENSP00000358470.3:n.-51C>A
ENST00000430871.3:c.-51C>A	ENSP00000484316.1:n.-51C>A
ENST00000463461.5:n.22C>A
NM_001253850.1:c.-51C>A	NP_001240779.1:n.-51C>A
NM_024626.3:c.-51C>A	NP_078902.2:n.-51C>A
NR_045603.1:n.55C>A
NR_045604.1:n.55C>A
XM_011542144.1:c.87-40735C>A	XP_011540446.1:n.87-40735C>A
XM_017002335.2:c.-314C>A	XP_016857824.1:n.-314C>A
NM_024626.4:c.-51C>A MANE Select	NP_078902.2:n.-51C>A
NR_045603.2:n.22C>A
NR_045604.2:n.22C>A
NM_001253850.2:c.-51C>A	NP_001240779.1:n.-51C>A