Canonical Allele Identifier: CA341808245

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690346A>T (hg19) ; chr1:g.117147724A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147724A>T , CM000663.2:g.117147724A>T	GRCh38
NC_000001.10:g.117690346A>T , CM000663.1:g.117690346A>T	GRCh37
NC_000001.9:g.117491869A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.783T>A MANE Select	ENSP00000358470.3:p.Cys261Ter
ENST00000328189.7:c.435T>A	ENSP00000328168.3:p.Cys145Ter
ENST00000359008.8:c.792T>A	ENSP00000351899.4:p.Cys264Ter
ENST00000369458.7:c.783T>A	ENSP00000358470.3:p.Cys261Ter
ENST00000539893.5:c.498T>A	ENSP00000444724.1:p.Cys166Ter
NM_001253849.1:c.498T>A	NP_001240778.1:p.Cys166Ter
NM_001253850.1:c.435T>A	NP_001240779.1:p.Cys145Ter
NM_024626.3:c.783T>A	NP_078902.2:p.Cys261Ter
NR_045603.1:n.978T>A
NR_045604.1:n.682T>A
XM_011542143.1:c.834T>A	XP_011540445.1:p.Cys278Ter
XM_011542144.1:c.837T>A	XP_011540446.1:p.Cys279Ter
XM_011542145.1:c.798T>A	XP_011540447.1:p.Cys266Ter
XM_011542143.2:c.933T>A	XP_011540445.2:p.Cys311Ter
XM_017002335.2:c.798T>A	XP_016857824.1:p.Cys266Ter
NM_024626.4:c.783T>A MANE Select	NP_078902.2:p.Cys261Ter
NR_045603.2:n.945T>A
NR_045604.2:n.649T>A
NM_001253849.2:c.498T>A	NP_001240778.1:p.Cys166Ter
NM_001253850.2:c.435T>A	NP_001240779.1:p.Cys145Ter