Canonical Allele Identifier: CA341808236

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690344A>T (hg19) ; chr1:g.117147722A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.785T>A MANE Select	ENSP00000358470.3:p.Val262Asp
ENST00000328189.7:c.437T>A	ENSP00000328168.3:p.Val146Asp
ENST00000359008.8:c.794T>A	ENSP00000351899.4:p.Val265Asp
ENST00000369458.7:c.785T>A	ENSP00000358470.3:p.Val262Asp
ENST00000539893.5:c.500T>A	ENSP00000444724.1:p.Val167Asp
NM_001253849.1:c.500T>A	NP_001240778.1:p.Val167Asp
NM_001253850.1:c.437T>A	NP_001240779.1:p.Val146Asp
NM_024626.3:c.785T>A	NP_078902.2:p.Val262Asp
NR_045603.1:n.980T>A
NR_045604.1:n.684T>A
XM_011542143.1:c.836T>A	XP_011540445.1:p.Val279Asp
XM_011542144.1:c.839T>A	XP_011540446.1:p.Val280Asp
XM_011542145.1:c.800T>A	XP_011540447.1:p.Val267Asp
XM_011542143.2:c.935T>A	XP_011540445.2:p.Val312Asp
XM_017002335.2:c.800T>A	XP_016857824.1:p.Val267Asp
NM_024626.4:c.785T>A MANE Select	NP_078902.2:p.Val262Asp
NR_045603.2:n.947T>A
NR_045604.2:n.651T>A
NM_001253849.2:c.500T>A	NP_001240778.1:p.Val167Asp
NM_001253850.2:c.437T>A	NP_001240779.1:p.Val146Asp