Canonical Allele Identifier: CA341807990

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690280T>A (hg19) ; chr1:g.117147658T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.849A>T MANE Select	ENSP00000358470.3:p.Ter283Tyr
ENST00000328189.7:c.501A>T	ENSP00000328168.3:p.Ter167Tyr
ENST00000359008.8:c.858A>T	ENSP00000351899.4:p.Ter286Tyr
ENST00000369458.7:c.849A>T	ENSP00000358470.3:p.Ter283Tyr
ENST00000539893.5:c.564A>T	ENSP00000444724.1:p.Ter188Tyr
NM_001253849.1:c.564A>T	NP_001240778.1:p.Ter188Tyr
NM_001253850.1:c.501A>T	NP_001240779.1:p.Ter167Tyr
NM_024626.3:c.849A>T	NP_078902.2:p.Ter283Tyr
NR_045603.1:n.1044A>T
NR_045604.1:n.748A>T
XM_011542143.1:c.900A>T	XP_011540445.1:p.Ter300Tyr
XM_011542144.1:c.903A>T	XP_011540446.1:p.Ter301Tyr
XM_011542145.1:c.864A>T	XP_011540447.1:p.Ter288Tyr
XM_011542143.2:c.999A>T	XP_011540445.2:p.Ter333Tyr
XM_017002335.2:c.864A>T	XP_016857824.1:p.Ter288Tyr
NM_024626.4:c.849A>T MANE Select	NP_078902.2:p.Ter283Tyr
NR_045603.2:n.1011A>T
NR_045604.2:n.715A>T
NM_001253849.2:c.564A>T	NP_001240778.1:p.Ter188Tyr
NM_001253850.2:c.501A>T	NP_001240779.1:p.Ter167Tyr