Canonical Allele Identifier: CA419932370

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690331A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147709A>G , CM000663.2:g.117147709A>G	GRCh38
NC_000001.10:g.117690331A>G , CM000663.1:g.117690331A>G	GRCh37
NC_000001.9:g.117491854A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.798T>C MANE Select	ENSP00000358470.3:p.Phe266=
ENST00000328189.7:c.450T>C	ENSP00000328168.3:p.Phe150=
ENST00000359008.8:c.807T>C	ENSP00000351899.4:p.Phe269=
ENST00000369458.7:c.798T>C	ENSP00000358470.3:p.Phe266=
ENST00000539893.5:c.513T>C	ENSP00000444724.1:p.Phe171=
NM_001253849.1:c.513T>C	NP_001240778.1:p.Phe171=
NM_001253850.1:c.450T>C	NP_001240779.1:p.Phe150=
NM_024626.3:c.798T>C	NP_078902.2:p.Phe266=
NR_045603.1:n.993T>C
NR_045604.1:n.697T>C
XM_011542143.1:c.849T>C	XP_011540445.1:p.Phe283=
XM_011542144.1:c.852T>C	XP_011540446.1:p.Phe284=
XM_011542145.1:c.813T>C	XP_011540447.1:p.Phe271=
XM_011542143.2:c.948T>C	XP_011540445.2:p.Phe316=
XM_017002335.2:c.813T>C	XP_016857824.1:p.Phe271=
NM_024626.4:c.798T>C MANE Select	NP_078902.2:p.Phe266=
NR_045603.2:n.960T>C
NR_045604.2:n.664T>C
NM_001253849.2:c.513T>C	NP_001240778.1:p.Phe171=
NM_001253850.2:c.450T>C	NP_001240779.1:p.Phe150=