Canonical Allele Identifier: CA341808159

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690326A>T (hg19) ; chr1:g.117147704A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147704A>T , CM000663.2:g.117147704A>T	GRCh38
NC_000001.10:g.117690326A>T , CM000663.1:g.117690326A>T	GRCh37
NC_000001.9:g.117491849A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.803T>A MANE Select	ENSP00000358470.3:p.Ile268Asn
ENST00000328189.7:c.455T>A	ENSP00000328168.3:p.Ile152Asn
ENST00000359008.8:c.812T>A	ENSP00000351899.4:p.Ile271Asn
ENST00000369458.7:c.803T>A	ENSP00000358470.3:p.Ile268Asn
ENST00000539893.5:c.518T>A	ENSP00000444724.1:p.Ile173Asn
NM_001253849.1:c.518T>A	NP_001240778.1:p.Ile173Asn
NM_001253850.1:c.455T>A	NP_001240779.1:p.Ile152Asn
NM_024626.3:c.803T>A	NP_078902.2:p.Ile268Asn
NR_045603.1:n.998T>A
NR_045604.1:n.702T>A
XM_011542143.1:c.854T>A	XP_011540445.1:p.Ile285Asn
XM_011542144.1:c.857T>A	XP_011540446.1:p.Ile286Asn
XM_011542145.1:c.818T>A	XP_011540447.1:p.Ile273Asn
XM_011542143.2:c.953T>A	XP_011540445.2:p.Ile318Asn
XM_017002335.2:c.818T>A	XP_016857824.1:p.Ile273Asn
NM_024626.4:c.803T>A MANE Select	NP_078902.2:p.Ile268Asn
NR_045603.2:n.965T>A
NR_045604.2:n.669T>A
NM_001253849.2:c.518T>A	NP_001240778.1:p.Ile173Asn
NM_001253850.2:c.455T>A	NP_001240779.1:p.Ile152Asn