Canonical Allele Identifier: CA419932371

Gene: VTCN1

Linked Data

• dbSNP Id: rs2101423047
• gnomAD v4: 1-117147712-G-A
• MyVariant Identifiers: chr1:g.117690334G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.795C>T MANE Select	ENSP00000358470.3:p.Phe265=
ENST00000328189.7:c.447C>T	ENSP00000328168.3:p.Phe149=
ENST00000359008.8:c.804C>T	ENSP00000351899.4:p.Phe268=
ENST00000369458.7:c.795C>T	ENSP00000358470.3:p.Phe265=
ENST00000539893.5:c.510C>T	ENSP00000444724.1:p.Phe170=
NM_001253849.1:c.510C>T	NP_001240778.1:p.Phe170=
NM_001253850.1:c.447C>T	NP_001240779.1:p.Phe149=
NM_024626.3:c.795C>T	NP_078902.2:p.Phe265=
NR_045603.1:n.990C>T
NR_045604.1:n.694C>T
XM_011542143.1:c.846C>T	XP_011540445.1:p.Phe282=
XM_011542144.1:c.849C>T	XP_011540446.1:p.Phe283=
XM_011542145.1:c.810C>T	XP_011540447.1:p.Phe270=
XM_011542143.2:c.945C>T	XP_011540445.2:p.Phe315=
XM_017002335.2:c.810C>T	XP_016857824.1:p.Phe270=
NM_024626.4:c.795C>T MANE Select	NP_078902.2:p.Phe265=
NR_045603.2:n.957C>T
NR_045604.2:n.661C>T
NM_001253849.2:c.510C>T	NP_001240778.1:p.Phe170=
NM_001253850.2:c.447C>T	NP_001240779.1:p.Phe149=