Canonical Allele Identifier: CA341808283

Gene: VTCN1

Linked Data

• gnomAD v4: 1-117147735-C-T
• MyVariant Identifiers: chr1:g.117690357C>T (hg19) ; chr1:g.117147735C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147735C>T , CM000663.2:g.117147735C>T	GRCh38
NC_000001.10:g.117690357C>T , CM000663.1:g.117690357C>T	GRCh37
NC_000001.9:g.117491880C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.772G>A MANE Select	ENSP00000358470.3:p.Ala258Thr
ENST00000328189.7:c.424G>A	ENSP00000328168.3:p.Ala142Thr
ENST00000359008.8:c.781G>A	ENSP00000351899.4:p.Ala261Thr
ENST00000369458.7:c.772G>A	ENSP00000358470.3:p.Ala258Thr
ENST00000539893.5:c.487G>A	ENSP00000444724.1:p.Ala163Thr
NM_001253849.1:c.487G>A	NP_001240778.1:p.Ala163Thr
NM_001253850.1:c.424G>A	NP_001240779.1:p.Ala142Thr
NM_024626.3:c.772G>A	NP_078902.2:p.Ala258Thr
NR_045603.1:n.967G>A
NR_045604.1:n.671G>A
XM_011542143.1:c.823G>A	XP_011540445.1:p.Ala275Thr
XM_011542144.1:c.826G>A	XP_011540446.1:p.Ala276Thr
XM_011542145.1:c.787G>A	XP_011540447.1:p.Ala263Thr
XM_011542143.2:c.922G>A	XP_011540445.2:p.Ala308Thr
XM_017002335.2:c.787G>A	XP_016857824.1:p.Ala263Thr
NM_024626.4:c.772G>A MANE Select	NP_078902.2:p.Ala258Thr
NR_045603.2:n.934G>A
NR_045604.2:n.638G>A
NM_001253849.2:c.487G>A	NP_001240778.1:p.Ala163Thr
NM_001253850.2:c.424G>A	NP_001240779.1:p.Ala142Thr