Canonical Allele Identifier: CA341808176

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690330C>T (hg19) ; chr1:g.117147708C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147708C>T , CM000663.2:g.117147708C>T	GRCh38
NC_000001.10:g.117690330C>T , CM000663.1:g.117690330C>T	GRCh37
NC_000001.9:g.117491853C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.799G>A MANE Select	ENSP00000358470.3:p.Ala267Thr
ENST00000328189.7:c.451G>A	ENSP00000328168.3:p.Ala151Thr
ENST00000359008.8:c.808G>A	ENSP00000351899.4:p.Ala270Thr
ENST00000369458.7:c.799G>A	ENSP00000358470.3:p.Ala267Thr
ENST00000539893.5:c.514G>A	ENSP00000444724.1:p.Ala172Thr
NM_001253849.1:c.514G>A	NP_001240778.1:p.Ala172Thr
NM_001253850.1:c.451G>A	NP_001240779.1:p.Ala151Thr
NM_024626.3:c.799G>A	NP_078902.2:p.Ala267Thr
NR_045603.1:n.994G>A
NR_045604.1:n.698G>A
XM_011542143.1:c.850G>A	XP_011540445.1:p.Ala284Thr
XM_011542144.1:c.853G>A	XP_011540446.1:p.Ala285Thr
XM_011542145.1:c.814G>A	XP_011540447.1:p.Ala272Thr
XM_011542143.2:c.949G>A	XP_011540445.2:p.Ala317Thr
XM_017002335.2:c.814G>A	XP_016857824.1:p.Ala272Thr
NM_024626.4:c.799G>A MANE Select	NP_078902.2:p.Ala267Thr
NR_045603.2:n.961G>A
NR_045604.2:n.665G>A
NM_001253849.2:c.514G>A	NP_001240778.1:p.Ala172Thr
NM_001253850.2:c.451G>A	NP_001240779.1:p.Ala151Thr