Canonical Allele Identifier: CA341808200

Gene: VTCN1

Linked Data

• gnomAD v4: 1-117147713-A-G
• MyVariant Identifiers: chr1:g.117690335A>G (hg19) ; chr1:g.117147713A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147713A>G , CM000663.2:g.117147713A>G	GRCh38
NC_000001.10:g.117690335A>G , CM000663.1:g.117690335A>G	GRCh37
NC_000001.9:g.117491858A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.794T>C MANE Select	ENSP00000358470.3:p.Phe265Ser
ENST00000328189.7:c.446T>C	ENSP00000328168.3:p.Phe149Ser
ENST00000359008.8:c.803T>C	ENSP00000351899.4:p.Phe268Ser
ENST00000369458.7:c.794T>C	ENSP00000358470.3:p.Phe265Ser
ENST00000539893.5:c.509T>C	ENSP00000444724.1:p.Phe170Ser
NM_001253849.1:c.509T>C	NP_001240778.1:p.Phe170Ser
NM_001253850.1:c.446T>C	NP_001240779.1:p.Phe149Ser
NM_024626.3:c.794T>C	NP_078902.2:p.Phe265Ser
NR_045603.1:n.989T>C
NR_045604.1:n.693T>C
XM_011542143.1:c.845T>C	XP_011540445.1:p.Phe282Ser
XM_011542144.1:c.848T>C	XP_011540446.1:p.Phe283Ser
XM_011542145.1:c.809T>C	XP_011540447.1:p.Phe270Ser
XM_011542143.2:c.944T>C	XP_011540445.2:p.Phe315Ser
XM_017002335.2:c.809T>C	XP_016857824.1:p.Phe270Ser
NM_024626.4:c.794T>C MANE Select	NP_078902.2:p.Phe265Ser
NR_045603.2:n.956T>C
NR_045604.2:n.660T>C
NM_001253849.2:c.509T>C	NP_001240778.1:p.Phe170Ser
NM_001253850.2:c.446T>C	NP_001240779.1:p.Phe149Ser