Canonical Allele Identifier: CA419932302

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690283T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147661T>C , CM000663.2:g.117147661T>C	GRCh38
NC_000001.10:g.117690283T>C , CM000663.1:g.117690283T>C	GRCh37
NC_000001.9:g.117491806T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.846A>G MANE Select	ENSP00000358470.3:p.Lys282=
ENST00000328189.7:c.498A>G	ENSP00000328168.3:p.Lys166=
ENST00000359008.8:c.855A>G	ENSP00000351899.4:p.Lys285=
ENST00000369458.7:c.846A>G	ENSP00000358470.3:p.Lys282=
ENST00000539893.5:c.561A>G	ENSP00000444724.1:p.Lys187=
NM_001253849.1:c.561A>G	NP_001240778.1:p.Lys187=
NM_001253850.1:c.498A>G	NP_001240779.1:p.Lys166=
NM_024626.3:c.846A>G	NP_078902.2:p.Lys282=
NR_045603.1:n.1041A>G
NR_045604.1:n.745A>G
XM_011542143.1:c.897A>G	XP_011540445.1:p.Lys299=
XM_011542144.1:c.900A>G	XP_011540446.1:p.Lys300=
XM_011542145.1:c.861A>G	XP_011540447.1:p.Lys287=
XM_011542143.2:c.996A>G	XP_011540445.2:p.Lys332=
XM_017002335.2:c.861A>G	XP_016857824.1:p.Lys287=
NM_024626.4:c.846A>G MANE Select	NP_078902.2:p.Lys282=
NR_045603.2:n.1008A>G
NR_045604.2:n.712A>G
NM_001253849.2:c.561A>G	NP_001240778.1:p.Lys187=
NM_001253850.2:c.498A>G	NP_001240779.1:p.Lys166=