Canonical Allele Identifier: CA419932366

Gene: VTCN1

Linked Data

• dbSNP Id: rs369356108
• MyVariant Identifiers: chr1:g.117690328G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147706G>T , CM000663.2:g.117147706G>T	GRCh38
NC_000001.10:g.117690328G>T , CM000663.1:g.117690328G>T	GRCh37
NC_000001.9:g.117491851G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.801C>A MANE Select	ENSP00000358470.3:p.Ala267=
ENST00000328189.7:c.453C>A	ENSP00000328168.3:p.Ala151=
ENST00000359008.8:c.810C>A	ENSP00000351899.4:p.Ala270=
ENST00000369458.7:c.801C>A	ENSP00000358470.3:p.Ala267=
ENST00000539893.5:c.516C>A	ENSP00000444724.1:p.Ala172=
NM_001253849.1:c.516C>A	NP_001240778.1:p.Ala172=
NM_001253850.1:c.453C>A	NP_001240779.1:p.Ala151=
NM_024626.3:c.801C>A	NP_078902.2:p.Ala267=
NR_045603.1:n.996C>A
NR_045604.1:n.700C>A
XM_011542143.1:c.852C>A	XP_011540445.1:p.Ala284=
XM_011542144.1:c.855C>A	XP_011540446.1:p.Ala285=
XM_011542145.1:c.816C>A	XP_011540447.1:p.Ala272=
XM_011542143.2:c.951C>A	XP_011540445.2:p.Ala317=
XM_017002335.2:c.816C>A	XP_016857824.1:p.Ala272=
NM_024626.4:c.801C>A MANE Select	NP_078902.2:p.Ala267=
NR_045603.2:n.963C>A
NR_045604.2:n.667C>A
NM_001253849.2:c.516C>A	NP_001240778.1:p.Ala172=
NM_001253850.2:c.453C>A	NP_001240779.1:p.Ala151=