Canonical Allele Identifier: CA341808069

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690303T>G (hg19) ; chr1:g.117147681T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147681T>G , CM000663.2:g.117147681T>G	GRCh38
NC_000001.10:g.117690303T>G , CM000663.1:g.117690303T>G	GRCh37
NC_000001.9:g.117491826T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.826A>C MANE Select	ENSP00000358470.3:p.Ser276Arg
ENST00000328189.7:c.478A>C	ENSP00000328168.3:p.Ser160Arg
ENST00000359008.8:c.835A>C	ENSP00000351899.4:p.Ser279Arg
ENST00000369458.7:c.826A>C	ENSP00000358470.3:p.Ser276Arg
ENST00000539893.5:c.541A>C	ENSP00000444724.1:p.Ser181Arg
NM_001253849.1:c.541A>C	NP_001240778.1:p.Ser181Arg
NM_001253850.1:c.478A>C	NP_001240779.1:p.Ser160Arg
NM_024626.3:c.826A>C	NP_078902.2:p.Ser276Arg
NR_045603.1:n.1021A>C
NR_045604.1:n.725A>C
XM_011542143.1:c.877A>C	XP_011540445.1:p.Ser293Arg
XM_011542144.1:c.880A>C	XP_011540446.1:p.Ser294Arg
XM_011542145.1:c.841A>C	XP_011540447.1:p.Ser281Arg
XM_011542143.2:c.976A>C	XP_011540445.2:p.Ser326Arg
XM_017002335.2:c.841A>C	XP_016857824.1:p.Ser281Arg
NM_024626.4:c.826A>C MANE Select	NP_078902.2:p.Ser276Arg
NR_045603.2:n.988A>C
NR_045604.2:n.692A>C
NM_001253849.2:c.541A>C	NP_001240778.1:p.Ser181Arg
NM_001253850.2:c.478A>C	NP_001240779.1:p.Ser160Arg