Canonical Allele Identifier: CA419932405

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690352A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147730A>T , CM000663.2:g.117147730A>T	GRCh38
NC_000001.10:g.117690352A>T , CM000663.1:g.117690352A>T	GRCh37
NC_000001.9:g.117491875A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.777T>A MANE Select	ENSP00000358470.3:p.Ser259=
ENST00000328189.7:c.429T>A	ENSP00000328168.3:p.Ser143=
ENST00000359008.8:c.786T>A	ENSP00000351899.4:p.Ser262=
ENST00000369458.7:c.777T>A	ENSP00000358470.3:p.Ser259=
ENST00000539893.5:c.492T>A	ENSP00000444724.1:p.Ser164=
NM_001253849.1:c.492T>A	NP_001240778.1:p.Ser164=
NM_001253850.1:c.429T>A	NP_001240779.1:p.Ser143=
NM_024626.3:c.777T>A	NP_078902.2:p.Ser259=
NR_045603.1:n.972T>A
NR_045604.1:n.676T>A
XM_011542143.1:c.828T>A	XP_011540445.1:p.Ser276=
XM_011542144.1:c.831T>A	XP_011540446.1:p.Ser277=
XM_011542145.1:c.792T>A	XP_011540447.1:p.Ser264=
XM_011542143.2:c.927T>A	XP_011540445.2:p.Ser309=
XM_017002335.2:c.792T>A	XP_016857824.1:p.Ser264=
NM_024626.4:c.777T>A MANE Select	NP_078902.2:p.Ser259=
NR_045603.2:n.939T>A
NR_045604.2:n.643T>A
NM_001253849.2:c.492T>A	NP_001240778.1:p.Ser164=
NM_001253850.2:c.429T>A	NP_001240779.1:p.Ser143=