Canonical Allele Identifier: CA419932348

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690312G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147690G>A , CM000663.2:g.117147690G>A	GRCh38
NC_000001.10:g.117690312G>A , CM000663.1:g.117690312G>A	GRCh37
NC_000001.9:g.117491835G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.817C>T MANE Select	ENSP00000358470.3:p.Leu273=
ENST00000328189.7:c.469C>T	ENSP00000328168.3:p.Leu157=
ENST00000359008.8:c.826C>T	ENSP00000351899.4:p.Leu276=
ENST00000369458.7:c.817C>T	ENSP00000358470.3:p.Leu273=
ENST00000539893.5:c.532C>T	ENSP00000444724.1:p.Leu178=
NM_001253849.1:c.532C>T	NP_001240778.1:p.Leu178=
NM_001253850.1:c.469C>T	NP_001240779.1:p.Leu157=
NM_024626.3:c.817C>T	NP_078902.2:p.Leu273=
NR_045603.1:n.1012C>T
NR_045604.1:n.716C>T
XM_011542143.1:c.868C>T	XP_011540445.1:p.Leu290=
XM_011542144.1:c.871C>T	XP_011540446.1:p.Leu291=
XM_011542145.1:c.832C>T	XP_011540447.1:p.Leu278=
XM_011542143.2:c.967C>T	XP_011540445.2:p.Leu323=
XM_017002335.2:c.832C>T	XP_016857824.1:p.Leu278=
NM_024626.4:c.817C>T MANE Select	NP_078902.2:p.Leu273=
NR_045603.2:n.979C>T
NR_045604.2:n.683C>T
NM_001253849.2:c.532C>T	NP_001240778.1:p.Leu178=
NM_001253850.2:c.469C>T	NP_001240779.1:p.Leu157=