Canonical Allele Identifier: CA419932399

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690349C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147727C>A , CM000663.2:g.117147727C>A	GRCh38
NC_000001.10:g.117690349C>A , CM000663.1:g.117690349C>A	GRCh37
NC_000001.9:g.117491872C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.780G>T MANE Select	ENSP00000358470.3:p.Leu260=
ENST00000328189.7:c.432G>T	ENSP00000328168.3:p.Leu144=
ENST00000359008.8:c.789G>T	ENSP00000351899.4:p.Leu263=
ENST00000369458.7:c.780G>T	ENSP00000358470.3:p.Leu260=
ENST00000539893.5:c.495G>T	ENSP00000444724.1:p.Leu165=
NM_001253849.1:c.495G>T	NP_001240778.1:p.Leu165=
NM_001253850.1:c.432G>T	NP_001240779.1:p.Leu144=
NM_024626.3:c.780G>T	NP_078902.2:p.Leu260=
NR_045603.1:n.975G>T
NR_045604.1:n.679G>T
XM_011542143.1:c.831G>T	XP_011540445.1:p.Leu277=
XM_011542144.1:c.834G>T	XP_011540446.1:p.Leu278=
XM_011542145.1:c.795G>T	XP_011540447.1:p.Leu265=
XM_011542143.2:c.930G>T	XP_011540445.2:p.Leu310=
XM_017002335.2:c.795G>T	XP_016857824.1:p.Leu265=
NM_024626.4:c.780G>T MANE Select	NP_078902.2:p.Leu260=
NR_045603.2:n.942G>T
NR_045604.2:n.646G>T
NM_001253849.2:c.495G>T	NP_001240778.1:p.Leu165=
NM_001253850.2:c.432G>T	NP_001240779.1:p.Leu144=