Canonical Allele Identifier: CA419932295

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690280T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147658T>C , CM000663.2:g.117147658T>C	GRCh38
NC_000001.10:g.117690280T>C , CM000663.1:g.117690280T>C	GRCh37
NC_000001.9:g.117491803T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.849A>G MANE Select	ENSP00000358470.3:p.Ter283=
ENST00000328189.7:c.501A>G	ENSP00000328168.3:p.Ter167=
ENST00000359008.8:c.858A>G	ENSP00000351899.4:p.Ter286=
ENST00000369458.7:c.849A>G	ENSP00000358470.3:p.Ter283=
ENST00000539893.5:c.564A>G	ENSP00000444724.1:p.Ter188=
NM_001253849.1:c.564A>G	NP_001240778.1:p.Ter188=
NM_001253850.1:c.501A>G	NP_001240779.1:p.Ter167=
NM_024626.3:c.849A>G	NP_078902.2:p.Ter283=
NR_045603.1:n.1044A>G
NR_045604.1:n.748A>G
XM_011542143.1:c.900A>G	XP_011540445.1:p.Ter300=
XM_011542144.1:c.903A>G	XP_011540446.1:p.Ter301=
XM_011542145.1:c.864A>G	XP_011540447.1:p.Ter288=
XM_011542143.2:c.999A>G	XP_011540445.2:p.Ter333=
XM_017002335.2:c.864A>G	XP_016857824.1:p.Ter288=
NM_024626.4:c.849A>G MANE Select	NP_078902.2:p.Ter283=
NR_045603.2:n.1011A>G
NR_045604.2:n.715A>G
NM_001253849.2:c.564A>G	NP_001240778.1:p.Ter188=
NM_001253850.2:c.501A>G	NP_001240779.1:p.Ter167=