Canonical Allele Identifier: CA341808268

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690354A>C (hg19) ; chr1:g.117147732A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147732A>C , CM000663.2:g.117147732A>C	GRCh38
NC_000001.10:g.117690354A>C , CM000663.1:g.117690354A>C	GRCh37
NC_000001.9:g.117491877A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.775T>G MANE Select	ENSP00000358470.3:p.Ser259Ala
ENST00000328189.7:c.427T>G	ENSP00000328168.3:p.Ser143Ala
ENST00000359008.8:c.784T>G	ENSP00000351899.4:p.Ser262Ala
ENST00000369458.7:c.775T>G	ENSP00000358470.3:p.Ser259Ala
ENST00000539893.5:c.490T>G	ENSP00000444724.1:p.Ser164Ala
NM_001253849.1:c.490T>G	NP_001240778.1:p.Ser164Ala
NM_001253850.1:c.427T>G	NP_001240779.1:p.Ser143Ala
NM_024626.3:c.775T>G	NP_078902.2:p.Ser259Ala
NR_045603.1:n.970T>G
NR_045604.1:n.674T>G
XM_011542143.1:c.826T>G	XP_011540445.1:p.Ser276Ala
XM_011542144.1:c.829T>G	XP_011540446.1:p.Ser277Ala
XM_011542145.1:c.790T>G	XP_011540447.1:p.Ser264Ala
XM_011542143.2:c.925T>G	XP_011540445.2:p.Ser309Ala
XM_017002335.2:c.790T>G	XP_016857824.1:p.Ser264Ala
NM_024626.4:c.775T>G MANE Select	NP_078902.2:p.Ser259Ala
NR_045603.2:n.937T>G
NR_045604.2:n.641T>G
NM_001253849.2:c.490T>G	NP_001240778.1:p.Ser164Ala
NM_001253850.2:c.427T>G	NP_001240779.1:p.Ser143Ala