Canonical Allele Identifier: CA341808090

Gene: VTCN1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.820C>G MANE Select	ENSP00000358470.3:p.Pro274Ala
ENST00000328189.7:c.472C>G	ENSP00000328168.3:p.Pro158Ala
ENST00000359008.8:c.829C>G	ENSP00000351899.4:p.Pro277Ala
ENST00000369458.7:c.820C>G	ENSP00000358470.3:p.Pro274Ala
ENST00000539893.5:c.535C>G	ENSP00000444724.1:p.Pro179Ala
NM_001253849.1:c.535C>G	NP_001240778.1:p.Pro179Ala
NM_001253850.1:c.472C>G	NP_001240779.1:p.Pro158Ala
NM_024626.3:c.820C>G	NP_078902.2:p.Pro274Ala
NR_045603.1:n.1015C>G
NR_045604.1:n.719C>G
XM_011542143.1:c.871C>G	XP_011540445.1:p.Pro291Ala
XM_011542144.1:c.874C>G	XP_011540446.1:p.Pro292Ala
XM_011542145.1:c.835C>G	XP_011540447.1:p.Pro279Ala
XM_011542143.2:c.970C>G	XP_011540445.2:p.Pro324Ala
XM_017002335.2:c.835C>G	XP_016857824.1:p.Pro279Ala
NM_024626.4:c.820C>G MANE Select	NP_078902.2:p.Pro274Ala
NR_045603.2:n.982C>G
NR_045604.2:n.686C>G
NM_001253849.2:c.535C>G	NP_001240778.1:p.Pro179Ala
NM_001253850.2:c.472C>G	NP_001240779.1:p.Pro158Ala