Canonical Allele Identifier: CA419932388

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690343G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147721G>A , CM000663.2:g.117147721G>A	GRCh38
NC_000001.10:g.117690343G>A , CM000663.1:g.117690343G>A	GRCh37
NC_000001.9:g.117491866G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.786C>T MANE Select	ENSP00000358470.3:p.Val262=
ENST00000328189.7:c.438C>T	ENSP00000328168.3:p.Val146=
ENST00000359008.8:c.795C>T	ENSP00000351899.4:p.Val265=
ENST00000369458.7:c.786C>T	ENSP00000358470.3:p.Val262=
ENST00000539893.5:c.501C>T	ENSP00000444724.1:p.Val167=
NM_001253849.1:c.501C>T	NP_001240778.1:p.Val167=
NM_001253850.1:c.438C>T	NP_001240779.1:p.Val146=
NM_024626.3:c.786C>T	NP_078902.2:p.Val262=
NR_045603.1:n.981C>T
NR_045604.1:n.685C>T
XM_011542143.1:c.837C>T	XP_011540445.1:p.Val279=
XM_011542144.1:c.840C>T	XP_011540446.1:p.Val280=
XM_011542145.1:c.801C>T	XP_011540447.1:p.Val267=
XM_011542143.2:c.936C>T	XP_011540445.2:p.Val312=
XM_017002335.2:c.801C>T	XP_016857824.1:p.Val267=
NM_024626.4:c.786C>T MANE Select	NP_078902.2:p.Val262=
NR_045603.2:n.948C>T
NR_045604.2:n.652C>T
NM_001253849.2:c.501C>T	NP_001240778.1:p.Val167=
NM_001253850.2:c.438C>T	NP_001240779.1:p.Val146=