Canonical Allele Identifier: CA419932322

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690292C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147670C>G , CM000663.2:g.117147670C>G	GRCh38
NC_000001.10:g.117690292C>G , CM000663.1:g.117690292C>G	GRCh37
NC_000001.9:g.117491815C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.837G>C MANE Select	ENSP00000358470.3:p.Leu279=
ENST00000328189.7:c.489G>C	ENSP00000328168.3:p.Leu163=
ENST00000359008.8:c.846G>C	ENSP00000351899.4:p.Leu282=
ENST00000369458.7:c.837G>C	ENSP00000358470.3:p.Leu279=
ENST00000539893.5:c.552G>C	ENSP00000444724.1:p.Leu184=
NM_001253849.1:c.552G>C	NP_001240778.1:p.Leu184=
NM_001253850.1:c.489G>C	NP_001240779.1:p.Leu163=
NM_024626.3:c.837G>C	NP_078902.2:p.Leu279=
NR_045603.1:n.1032G>C
NR_045604.1:n.736G>C
XM_011542143.1:c.888G>C	XP_011540445.1:p.Leu296=
XM_011542144.1:c.891G>C	XP_011540446.1:p.Leu297=
XM_011542145.1:c.852G>C	XP_011540447.1:p.Leu284=
XM_011542143.2:c.987G>C	XP_011540445.2:p.Leu329=
XM_017002335.2:c.852G>C	XP_016857824.1:p.Leu284=
NM_024626.4:c.837G>C MANE Select	NP_078902.2:p.Leu279=
NR_045603.2:n.999G>C
NR_045604.2:n.703G>C
NM_001253849.2:c.552G>C	NP_001240778.1:p.Leu184=
NM_001253850.2:c.489G>C	NP_001240779.1:p.Leu163=