Canonical Allele Identifier: CA341808179

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690331A>C (hg19) ; chr1:g.117147709A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147709A>C , CM000663.2:g.117147709A>C	GRCh38
NC_000001.10:g.117690331A>C , CM000663.1:g.117690331A>C	GRCh37
NC_000001.9:g.117491854A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.798T>G MANE Select	ENSP00000358470.3:p.Phe266Leu
ENST00000328189.7:c.450T>G	ENSP00000328168.3:p.Phe150Leu
ENST00000359008.8:c.807T>G	ENSP00000351899.4:p.Phe269Leu
ENST00000369458.7:c.798T>G	ENSP00000358470.3:p.Phe266Leu
ENST00000539893.5:c.513T>G	ENSP00000444724.1:p.Phe171Leu
NM_001253849.1:c.513T>G	NP_001240778.1:p.Phe171Leu
NM_001253850.1:c.450T>G	NP_001240779.1:p.Phe150Leu
NM_024626.3:c.798T>G	NP_078902.2:p.Phe266Leu
NR_045603.1:n.993T>G
NR_045604.1:n.697T>G
XM_011542143.1:c.849T>G	XP_011540445.1:p.Phe283Leu
XM_011542144.1:c.852T>G	XP_011540446.1:p.Phe284Leu
XM_011542145.1:c.813T>G	XP_011540447.1:p.Phe271Leu
XM_011542143.2:c.948T>G	XP_011540445.2:p.Phe316Leu
XM_017002335.2:c.813T>G	XP_016857824.1:p.Phe271Leu
NM_024626.4:c.798T>G MANE Select	NP_078902.2:p.Phe266Leu
NR_045603.2:n.960T>G
NR_045604.2:n.664T>G
NM_001253849.2:c.513T>G	NP_001240778.1:p.Phe171Leu
NM_001253850.2:c.450T>G	NP_001240779.1:p.Phe150Leu