Canonical Allele Identifier: CA341808193

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690334G>C (hg19) ; chr1:g.117147712G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147712G>C , CM000663.2:g.117147712G>C	GRCh38
NC_000001.10:g.117690334G>C , CM000663.1:g.117690334G>C	GRCh37
NC_000001.9:g.117491857G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.795C>G MANE Select	ENSP00000358470.3:p.Phe265Leu
ENST00000328189.7:c.447C>G	ENSP00000328168.3:p.Phe149Leu
ENST00000359008.8:c.804C>G	ENSP00000351899.4:p.Phe268Leu
ENST00000369458.7:c.795C>G	ENSP00000358470.3:p.Phe265Leu
ENST00000539893.5:c.510C>G	ENSP00000444724.1:p.Phe170Leu
NM_001253849.1:c.510C>G	NP_001240778.1:p.Phe170Leu
NM_001253850.1:c.447C>G	NP_001240779.1:p.Phe149Leu
NM_024626.3:c.795C>G	NP_078902.2:p.Phe265Leu
NR_045603.1:n.990C>G
NR_045604.1:n.694C>G
XM_011542143.1:c.846C>G	XP_011540445.1:p.Phe282Leu
XM_011542144.1:c.849C>G	XP_011540446.1:p.Phe283Leu
XM_011542145.1:c.810C>G	XP_011540447.1:p.Phe270Leu
XM_011542143.2:c.945C>G	XP_011540445.2:p.Phe315Leu
XM_017002335.2:c.810C>G	XP_016857824.1:p.Phe270Leu
NM_024626.4:c.795C>G MANE Select	NP_078902.2:p.Phe265Leu
NR_045603.2:n.957C>G
NR_045604.2:n.661C>G
NM_001253849.2:c.510C>G	NP_001240778.1:p.Phe170Leu
NM_001253850.2:c.447C>G	NP_001240779.1:p.Phe149Leu