Canonical Allele Identifier: CA341808128

Gene: VTCN1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.809G>C MANE Select	ENSP00000358470.3:p.Trp270Ser
ENST00000328189.7:c.461G>C	ENSP00000328168.3:p.Trp154Ser
ENST00000359008.8:c.818G>C	ENSP00000351899.4:p.Trp273Ser
ENST00000369458.7:c.809G>C	ENSP00000358470.3:p.Trp270Ser
ENST00000539893.5:c.524G>C	ENSP00000444724.1:p.Trp175Ser
NM_001253849.1:c.524G>C	NP_001240778.1:p.Trp175Ser
NM_001253850.1:c.461G>C	NP_001240779.1:p.Trp154Ser
NM_024626.3:c.809G>C	NP_078902.2:p.Trp270Ser
NR_045603.1:n.1004G>C
NR_045604.1:n.708G>C
XM_011542143.1:c.860G>C	XP_011540445.1:p.Trp287Ser
XM_011542144.1:c.863G>C	XP_011540446.1:p.Trp288Ser
XM_011542145.1:c.824G>C	XP_011540447.1:p.Trp275Ser
XM_011542143.2:c.959G>C	XP_011540445.2:p.Trp320Ser
XM_017002335.2:c.824G>C	XP_016857824.1:p.Trp275Ser
NM_024626.4:c.809G>C MANE Select	NP_078902.2:p.Trp270Ser
NR_045603.2:n.971G>C
NR_045604.2:n.675G>C
NM_001253849.2:c.524G>C	NP_001240778.1:p.Trp175Ser
NM_001253850.2:c.461G>C	NP_001240779.1:p.Trp154Ser