Canonical Allele Identifier: CA341808066

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690302C>G (hg19) ; chr1:g.117147680C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147680C>G , CM000663.2:g.117147680C>G	GRCh38
NC_000001.10:g.117690302C>G , CM000663.1:g.117690302C>G	GRCh37
NC_000001.9:g.117491825C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.827G>C MANE Select	ENSP00000358470.3:p.Ser276Thr
ENST00000328189.7:c.479G>C	ENSP00000328168.3:p.Ser160Thr
ENST00000359008.8:c.836G>C	ENSP00000351899.4:p.Ser279Thr
ENST00000369458.7:c.827G>C	ENSP00000358470.3:p.Ser276Thr
ENST00000539893.5:c.542G>C	ENSP00000444724.1:p.Ser181Thr
NM_001253849.1:c.542G>C	NP_001240778.1:p.Ser181Thr
NM_001253850.1:c.479G>C	NP_001240779.1:p.Ser160Thr
NM_024626.3:c.827G>C	NP_078902.2:p.Ser276Thr
NR_045603.1:n.1022G>C
NR_045604.1:n.726G>C
XM_011542143.1:c.878G>C	XP_011540445.1:p.Ser293Thr
XM_011542144.1:c.881G>C	XP_011540446.1:p.Ser294Thr
XM_011542145.1:c.842G>C	XP_011540447.1:p.Ser281Thr
XM_011542143.2:c.977G>C	XP_011540445.2:p.Ser326Thr
XM_017002335.2:c.842G>C	XP_016857824.1:p.Ser281Thr
NM_024626.4:c.827G>C MANE Select	NP_078902.2:p.Ser276Thr
NR_045603.2:n.989G>C
NR_045604.2:n.693G>C
NM_001253849.2:c.542G>C	NP_001240778.1:p.Ser181Thr
NM_001253850.2:c.479G>C	NP_001240779.1:p.Ser160Thr