Canonical Allele Identifier: CA341808168

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690329G>T (hg19) ; chr1:g.117147707G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147707G>T , CM000663.2:g.117147707G>T	GRCh38
NC_000001.10:g.117690329G>T , CM000663.1:g.117690329G>T	GRCh37
NC_000001.9:g.117491852G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.800C>A MANE Select	ENSP00000358470.3:p.Ala267Asp
ENST00000328189.7:c.452C>A	ENSP00000328168.3:p.Ala151Asp
ENST00000359008.8:c.809C>A	ENSP00000351899.4:p.Ala270Asp
ENST00000369458.7:c.800C>A	ENSP00000358470.3:p.Ala267Asp
ENST00000539893.5:c.515C>A	ENSP00000444724.1:p.Ala172Asp
NM_001253849.1:c.515C>A	NP_001240778.1:p.Ala172Asp
NM_001253850.1:c.452C>A	NP_001240779.1:p.Ala151Asp
NM_024626.3:c.800C>A	NP_078902.2:p.Ala267Asp
NR_045603.1:n.995C>A
NR_045604.1:n.699C>A
XM_011542143.1:c.851C>A	XP_011540445.1:p.Ala284Asp
XM_011542144.1:c.854C>A	XP_011540446.1:p.Ala285Asp
XM_011542145.1:c.815C>A	XP_011540447.1:p.Ala272Asp
XM_011542143.2:c.950C>A	XP_011540445.2:p.Ala317Asp
XM_017002335.2:c.815C>A	XP_016857824.1:p.Ala272Asp
NM_024626.4:c.800C>A MANE Select	NP_078902.2:p.Ala267Asp
NR_045603.2:n.962C>A
NR_045604.2:n.666C>A
NM_001253849.2:c.515C>A	NP_001240778.1:p.Ala172Asp
NM_001253850.2:c.452C>A	NP_001240779.1:p.Ala151Asp