Canonical Allele Identifier: CA341808175

Gene: VTCN1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.799G>C MANE Select	ENSP00000358470.3:p.Ala267Pro
ENST00000328189.7:c.451G>C	ENSP00000328168.3:p.Ala151Pro
ENST00000359008.8:c.808G>C	ENSP00000351899.4:p.Ala270Pro
ENST00000369458.7:c.799G>C	ENSP00000358470.3:p.Ala267Pro
ENST00000539893.5:c.514G>C	ENSP00000444724.1:p.Ala172Pro
NM_001253849.1:c.514G>C	NP_001240778.1:p.Ala172Pro
NM_001253850.1:c.451G>C	NP_001240779.1:p.Ala151Pro
NM_024626.3:c.799G>C	NP_078902.2:p.Ala267Pro
NR_045603.1:n.994G>C
NR_045604.1:n.698G>C
XM_011542143.1:c.850G>C	XP_011540445.1:p.Ala284Pro
XM_011542144.1:c.853G>C	XP_011540446.1:p.Ala285Pro
XM_011542145.1:c.814G>C	XP_011540447.1:p.Ala272Pro
XM_011542143.2:c.949G>C	XP_011540445.2:p.Ala317Pro
XM_017002335.2:c.814G>C	XP_016857824.1:p.Ala272Pro
NM_024626.4:c.799G>C MANE Select	NP_078902.2:p.Ala267Pro
NR_045603.2:n.961G>C
NR_045604.2:n.665G>C
NM_001253849.2:c.514G>C	NP_001240778.1:p.Ala172Pro
NM_001253850.2:c.451G>C	NP_001240779.1:p.Ala151Pro