Canonical Allele Identifier: CA341808234

Gene: VTCN1

Linked Data

• gnomAD v4: 1-117147722-A-G
• MyVariant Identifiers: chr1:g.117690344A>G (hg19) ; chr1:g.117147722A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147722A>G , CM000663.2:g.117147722A>G	GRCh38
NC_000001.10:g.117690344A>G , CM000663.1:g.117690344A>G	GRCh37
NC_000001.9:g.117491867A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.785T>C MANE Select	ENSP00000358470.3:p.Val262Ala
ENST00000328189.7:c.437T>C	ENSP00000328168.3:p.Val146Ala
ENST00000359008.8:c.794T>C	ENSP00000351899.4:p.Val265Ala
ENST00000369458.7:c.785T>C	ENSP00000358470.3:p.Val262Ala
ENST00000539893.5:c.500T>C	ENSP00000444724.1:p.Val167Ala
NM_001253849.1:c.500T>C	NP_001240778.1:p.Val167Ala
NM_001253850.1:c.437T>C	NP_001240779.1:p.Val146Ala
NM_024626.3:c.785T>C	NP_078902.2:p.Val262Ala
NR_045603.1:n.980T>C
NR_045604.1:n.684T>C
XM_011542143.1:c.836T>C	XP_011540445.1:p.Val279Ala
XM_011542144.1:c.839T>C	XP_011540446.1:p.Val280Ala
XM_011542145.1:c.800T>C	XP_011540447.1:p.Val267Ala
XM_011542143.2:c.935T>C	XP_011540445.2:p.Val312Ala
XM_017002335.2:c.800T>C	XP_016857824.1:p.Val267Ala
NM_024626.4:c.785T>C MANE Select	NP_078902.2:p.Val262Ala
NR_045603.2:n.947T>C
NR_045604.2:n.651T>C
NM_001253849.2:c.500T>C	NP_001240778.1:p.Val167Ala
NM_001253850.2:c.437T>C	NP_001240779.1:p.Val146Ala