Canonical Allele Identifier: CA341808187

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690333A>C (hg19) ; chr1:g.117147711A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147711A>C , CM000663.2:g.117147711A>C	GRCh38
NC_000001.10:g.117690333A>C , CM000663.1:g.117690333A>C	GRCh37
NC_000001.9:g.117491856A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.796T>G MANE Select	ENSP00000358470.3:p.Phe266Val
ENST00000328189.7:c.448T>G	ENSP00000328168.3:p.Phe150Val
ENST00000359008.8:c.805T>G	ENSP00000351899.4:p.Phe269Val
ENST00000369458.7:c.796T>G	ENSP00000358470.3:p.Phe266Val
ENST00000539893.5:c.511T>G	ENSP00000444724.1:p.Phe171Val
NM_001253849.1:c.511T>G	NP_001240778.1:p.Phe171Val
NM_001253850.1:c.448T>G	NP_001240779.1:p.Phe150Val
NM_024626.3:c.796T>G	NP_078902.2:p.Phe266Val
NR_045603.1:n.991T>G
NR_045604.1:n.695T>G
XM_011542143.1:c.847T>G	XP_011540445.1:p.Phe283Val
XM_011542144.1:c.850T>G	XP_011540446.1:p.Phe284Val
XM_011542145.1:c.811T>G	XP_011540447.1:p.Phe271Val
XM_011542143.2:c.946T>G	XP_011540445.2:p.Phe316Val
XM_017002335.2:c.811T>G	XP_016857824.1:p.Phe271Val
NM_024626.4:c.796T>G MANE Select	NP_078902.2:p.Phe266Val
NR_045603.2:n.958T>G
NR_045604.2:n.662T>G
NM_001253849.2:c.511T>G	NP_001240778.1:p.Phe171Val
NM_001253850.2:c.448T>G	NP_001240779.1:p.Phe150Val