Canonical Allele Identifier: CA341808155

Gene: VTCN1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.803T>G MANE Select	ENSP00000358470.3:p.Ile268Ser
ENST00000328189.7:c.455T>G	ENSP00000328168.3:p.Ile152Ser
ENST00000359008.8:c.812T>G	ENSP00000351899.4:p.Ile271Ser
ENST00000369458.7:c.803T>G	ENSP00000358470.3:p.Ile268Ser
ENST00000539893.5:c.518T>G	ENSP00000444724.1:p.Ile173Ser
NM_001253849.1:c.518T>G	NP_001240778.1:p.Ile173Ser
NM_001253850.1:c.455T>G	NP_001240779.1:p.Ile152Ser
NM_024626.3:c.803T>G	NP_078902.2:p.Ile268Ser
NR_045603.1:n.998T>G
NR_045604.1:n.702T>G
XM_011542143.1:c.854T>G	XP_011540445.1:p.Ile285Ser
XM_011542144.1:c.857T>G	XP_011540446.1:p.Ile286Ser
XM_011542145.1:c.818T>G	XP_011540447.1:p.Ile273Ser
XM_011542143.2:c.953T>G	XP_011540445.2:p.Ile318Ser
XM_017002335.2:c.818T>G	XP_016857824.1:p.Ile273Ser
NM_024626.4:c.803T>G MANE Select	NP_078902.2:p.Ile268Ser
NR_045603.2:n.965T>G
NR_045604.2:n.669T>G
NM_001253849.2:c.518T>G	NP_001240778.1:p.Ile173Ser
NM_001253850.2:c.455T>G	NP_001240779.1:p.Ile152Ser