Canonical Allele Identifier: CA341808282

Gene: VTCN1

Linked Data

• dbSNP Id: rs1256055722
• gnomAD v4: 1-117147735-C-G
• MyVariant Identifiers: chr1:g.117690357C>G (hg19) ; chr1:g.117147735C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.772G>C MANE Select	ENSP00000358470.3:p.Ala258Pro
ENST00000328189.7:c.424G>C	ENSP00000328168.3:p.Ala142Pro
ENST00000359008.8:c.781G>C	ENSP00000351899.4:p.Ala261Pro
ENST00000369458.7:c.772G>C	ENSP00000358470.3:p.Ala258Pro
ENST00000539893.5:c.487G>C	ENSP00000444724.1:p.Ala163Pro
NM_001253849.1:c.487G>C	NP_001240778.1:p.Ala163Pro
NM_001253850.1:c.424G>C	NP_001240779.1:p.Ala142Pro
NM_024626.3:c.772G>C	NP_078902.2:p.Ala258Pro
NR_045603.1:n.967G>C
NR_045604.1:n.671G>C
XM_011542143.1:c.823G>C	XP_011540445.1:p.Ala275Pro
XM_011542144.1:c.826G>C	XP_011540446.1:p.Ala276Pro
XM_011542145.1:c.787G>C	XP_011540447.1:p.Ala263Pro
XM_011542143.2:c.922G>C	XP_011540445.2:p.Ala308Pro
XM_017002335.2:c.787G>C	XP_016857824.1:p.Ala263Pro
NM_024626.4:c.772G>C MANE Select	NP_078902.2:p.Ala258Pro
NR_045603.2:n.934G>C
NR_045604.2:n.638G>C
NM_001253849.2:c.487G>C	NP_001240778.1:p.Ala163Pro
NM_001253850.2:c.424G>C	NP_001240779.1:p.Ala142Pro