Canonical Allele Identifier: CA419932328

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690298A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147676A>T , CM000663.2:g.117147676A>T	GRCh38
NC_000001.10:g.117690298A>T , CM000663.1:g.117690298A>T	GRCh37
NC_000001.9:g.117491821A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.831T>A MANE Select	ENSP00000358470.3:p.Pro277=
ENST00000328189.7:c.483T>A	ENSP00000328168.3:p.Pro161=
ENST00000359008.8:c.840T>A	ENSP00000351899.4:p.Pro280=
ENST00000369458.7:c.831T>A	ENSP00000358470.3:p.Pro277=
ENST00000539893.5:c.546T>A	ENSP00000444724.1:p.Pro182=
NM_001253849.1:c.546T>A	NP_001240778.1:p.Pro182=
NM_001253850.1:c.483T>A	NP_001240779.1:p.Pro161=
NM_024626.3:c.831T>A	NP_078902.2:p.Pro277=
NR_045603.1:n.1026T>A
NR_045604.1:n.730T>A
XM_011542143.1:c.882T>A	XP_011540445.1:p.Pro294=
XM_011542144.1:c.885T>A	XP_011540446.1:p.Pro295=
XM_011542145.1:c.846T>A	XP_011540447.1:p.Pro282=
XM_011542143.2:c.981T>A	XP_011540445.2:p.Pro327=
XM_017002335.2:c.846T>A	XP_016857824.1:p.Pro282=
NM_024626.4:c.831T>A MANE Select	NP_078902.2:p.Pro277=
NR_045603.2:n.993T>A
NR_045604.2:n.697T>A
NM_001253849.2:c.546T>A	NP_001240778.1:p.Pro182=
NM_001253850.2:c.483T>A	NP_001240779.1:p.Pro161=