Canonical Allele Identifier: CA419932362

Gene: VTCN1

Linked Data

• COSMIC: COSM4657449
• MyVariant Identifiers: chr1:g.117690325G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147703G>A , CM000663.2:g.117147703G>A	GRCh38
NC_000001.10:g.117690325G>A , CM000663.1:g.117690325G>A	GRCh37
NC_000001.9:g.117491848G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.804C>T MANE Select	ENSP00000358470.3:p.Ile268=
ENST00000328189.7:c.456C>T	ENSP00000328168.3:p.Ile152=
ENST00000359008.8:c.813C>T	ENSP00000351899.4:p.Ile271=
ENST00000369458.7:c.804C>T	ENSP00000358470.3:p.Ile268=
ENST00000539893.5:c.519C>T	ENSP00000444724.1:p.Ile173=
NM_001253849.1:c.519C>T	NP_001240778.1:p.Ile173=
NM_001253850.1:c.456C>T	NP_001240779.1:p.Ile152=
NM_024626.3:c.804C>T	NP_078902.2:p.Ile268=
NR_045603.1:n.999C>T
NR_045604.1:n.703C>T
XM_011542143.1:c.855C>T	XP_011540445.1:p.Ile285=
XM_011542144.1:c.858C>T	XP_011540446.1:p.Ile286=
XM_011542145.1:c.819C>T	XP_011540447.1:p.Ile273=
XM_011542143.2:c.954C>T	XP_011540445.2:p.Ile318=
XM_017002335.2:c.819C>T	XP_016857824.1:p.Ile273=
NM_024626.4:c.804C>T MANE Select	NP_078902.2:p.Ile268=
NR_045603.2:n.966C>T
NR_045604.2:n.670C>T
NM_001253849.2:c.519C>T	NP_001240778.1:p.Ile173=
NM_001253850.2:c.456C>T	NP_001240779.1:p.Ile152=