Canonical Allele Identifier: CA341808130

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690320C>T (hg19) ; chr1:g.117147698C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147698C>T , CM000663.2:g.117147698C>T	GRCh38
NC_000001.10:g.117690320C>T , CM000663.1:g.117690320C>T	GRCh37
NC_000001.9:g.117491843C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.809G>A MANE Select	ENSP00000358470.3:p.Trp270Ter
ENST00000328189.7:c.461G>A	ENSP00000328168.3:p.Trp154Ter
ENST00000359008.8:c.818G>A	ENSP00000351899.4:p.Trp273Ter
ENST00000369458.7:c.809G>A	ENSP00000358470.3:p.Trp270Ter
ENST00000539893.5:c.524G>A	ENSP00000444724.1:p.Trp175Ter
NM_001253849.1:c.524G>A	NP_001240778.1:p.Trp175Ter
NM_001253850.1:c.461G>A	NP_001240779.1:p.Trp154Ter
NM_024626.3:c.809G>A	NP_078902.2:p.Trp270Ter
NR_045603.1:n.1004G>A
NR_045604.1:n.708G>A
XM_011542143.1:c.860G>A	XP_011540445.1:p.Trp287Ter
XM_011542144.1:c.863G>A	XP_011540446.1:p.Trp288Ter
XM_011542145.1:c.824G>A	XP_011540447.1:p.Trp275Ter
XM_011542143.2:c.959G>A	XP_011540445.2:p.Trp320Ter
XM_017002335.2:c.824G>A	XP_016857824.1:p.Trp275Ter
NM_024626.4:c.809G>A MANE Select	NP_078902.2:p.Trp270Ter
NR_045603.2:n.971G>A
NR_045604.2:n.675G>A
NM_001253849.2:c.524G>A	NP_001240778.1:p.Trp175Ter
NM_001253850.2:c.461G>A	NP_001240779.1:p.Trp154Ter