Canonical Allele Identifier: CA341808089

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690309G>A (hg19) ; chr1:g.117147687G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147687G>A , CM000663.2:g.117147687G>A	GRCh38
NC_000001.10:g.117690309G>A , CM000663.1:g.117690309G>A	GRCh37
NC_000001.9:g.117491832G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.820C>T MANE Select	ENSP00000358470.3:p.Pro274Ser
ENST00000328189.7:c.472C>T	ENSP00000328168.3:p.Pro158Ser
ENST00000359008.8:c.829C>T	ENSP00000351899.4:p.Pro277Ser
ENST00000369458.7:c.820C>T	ENSP00000358470.3:p.Pro274Ser
ENST00000539893.5:c.535C>T	ENSP00000444724.1:p.Pro179Ser
NM_001253849.1:c.535C>T	NP_001240778.1:p.Pro179Ser
NM_001253850.1:c.472C>T	NP_001240779.1:p.Pro158Ser
NM_024626.3:c.820C>T	NP_078902.2:p.Pro274Ser
NR_045603.1:n.1015C>T
NR_045604.1:n.719C>T
XM_011542143.1:c.871C>T	XP_011540445.1:p.Pro291Ser
XM_011542144.1:c.874C>T	XP_011540446.1:p.Pro292Ser
XM_011542145.1:c.835C>T	XP_011540447.1:p.Pro279Ser
XM_011542143.2:c.970C>T	XP_011540445.2:p.Pro324Ser
XM_017002335.2:c.835C>T	XP_016857824.1:p.Pro279Ser
NM_024626.4:c.820C>T MANE Select	NP_078902.2:p.Pro274Ser
NR_045603.2:n.982C>T
NR_045604.2:n.686C>T
NM_001253849.2:c.535C>T	NP_001240778.1:p.Pro179Ser
NM_001253850.2:c.472C>T	NP_001240779.1:p.Pro158Ser