Canonical Allele Identifier: CA341808111

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690315G>C (hg19) ; chr1:g.117147693G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147693G>C , CM000663.2:g.117147693G>C	GRCh38
NC_000001.10:g.117690315G>C , CM000663.1:g.117690315G>C	GRCh37
NC_000001.9:g.117491838G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.814C>G MANE Select	ENSP00000358470.3:p.Leu272Val
ENST00000328189.7:c.466C>G	ENSP00000328168.3:p.Leu156Val
ENST00000359008.8:c.823C>G	ENSP00000351899.4:p.Leu275Val
ENST00000369458.7:c.814C>G	ENSP00000358470.3:p.Leu272Val
ENST00000539893.5:c.529C>G	ENSP00000444724.1:p.Leu177Val
NM_001253849.1:c.529C>G	NP_001240778.1:p.Leu177Val
NM_001253850.1:c.466C>G	NP_001240779.1:p.Leu156Val
NM_024626.3:c.814C>G	NP_078902.2:p.Leu272Val
NR_045603.1:n.1009C>G
NR_045604.1:n.713C>G
XM_011542143.1:c.865C>G	XP_011540445.1:p.Leu289Val
XM_011542144.1:c.868C>G	XP_011540446.1:p.Leu290Val
XM_011542145.1:c.829C>G	XP_011540447.1:p.Leu277Val
XM_011542143.2:c.964C>G	XP_011540445.2:p.Leu322Val
XM_017002335.2:c.829C>G	XP_016857824.1:p.Leu277Val
NM_024626.4:c.814C>G MANE Select	NP_078902.2:p.Leu272Val
NR_045603.2:n.976C>G
NR_045604.2:n.680C>G
NM_001253849.2:c.529C>G	NP_001240778.1:p.Leu177Val
NM_001253850.2:c.466C>G	NP_001240779.1:p.Leu156Val