Canonical Allele Identifier: CA419932298

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690281T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147659T>C , CM000663.2:g.117147659T>C	GRCh38
NC_000001.10:g.117690281T>C , CM000663.1:g.117690281T>C	GRCh37
NC_000001.9:g.117491804T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.848A>G MANE Select	ENSP00000358470.3:p.Ter283=
ENST00000328189.7:c.500A>G	ENSP00000328168.3:p.Ter167=
ENST00000359008.8:c.857A>G	ENSP00000351899.4:p.Ter286=
ENST00000369458.7:c.848A>G	ENSP00000358470.3:p.Ter283=
ENST00000539893.5:c.563A>G	ENSP00000444724.1:p.Ter188=
NM_001253849.1:c.563A>G	NP_001240778.1:p.Ter188=
NM_001253850.1:c.500A>G	NP_001240779.1:p.Ter167=
NM_024626.3:c.848A>G	NP_078902.2:p.Ter283=
NR_045603.1:n.1043A>G
NR_045604.1:n.747A>G
XM_011542143.1:c.899A>G	XP_011540445.1:p.Ter300=
XM_011542144.1:c.902A>G	XP_011540446.1:p.Ter301=
XM_011542145.1:c.863A>G	XP_011540447.1:p.Ter288=
XM_011542143.2:c.998A>G	XP_011540445.2:p.Ter333=
XM_017002335.2:c.863A>G	XP_016857824.1:p.Ter288=
NM_024626.4:c.848A>G MANE Select	NP_078902.2:p.Ter283=
NR_045603.2:n.1010A>G
NR_045604.2:n.714A>G
NM_001253849.2:c.563A>G	NP_001240778.1:p.Ter188=
NM_001253850.2:c.500A>G	NP_001240779.1:p.Ter167=