Canonical Allele Identifier: CA341808020

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690288G>T (hg19) ; chr1:g.117147666G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147666G>T , CM000663.2:g.117147666G>T	GRCh38
NC_000001.10:g.117690288G>T , CM000663.1:g.117690288G>T	GRCh37
NC_000001.9:g.117491811G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.841C>A MANE Select	ENSP00000358470.3:p.Leu281Ile
ENST00000328189.7:c.493C>A	ENSP00000328168.3:p.Leu165Ile
ENST00000359008.8:c.850C>A	ENSP00000351899.4:p.Leu284Ile
ENST00000369458.7:c.841C>A	ENSP00000358470.3:p.Leu281Ile
ENST00000539893.5:c.556C>A	ENSP00000444724.1:p.Leu186Ile
NM_001253849.1:c.556C>A	NP_001240778.1:p.Leu186Ile
NM_001253850.1:c.493C>A	NP_001240779.1:p.Leu165Ile
NM_024626.3:c.841C>A	NP_078902.2:p.Leu281Ile
NR_045603.1:n.1036C>A
NR_045604.1:n.740C>A
XM_011542143.1:c.892C>A	XP_011540445.1:p.Leu298Ile
XM_011542144.1:c.895C>A	XP_011540446.1:p.Leu299Ile
XM_011542145.1:c.856C>A	XP_011540447.1:p.Leu286Ile
XM_011542143.2:c.991C>A	XP_011540445.2:p.Leu331Ile
XM_017002335.2:c.856C>A	XP_016857824.1:p.Leu286Ile
NM_024626.4:c.841C>A MANE Select	NP_078902.2:p.Leu281Ile
NR_045603.2:n.1003C>A
NR_045604.2:n.707C>A
NM_001253849.2:c.556C>A	NP_001240778.1:p.Leu186Ile
NM_001253850.2:c.493C>A	NP_001240779.1:p.Leu165Ile