Canonical Allele Identifier: CA341807997

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690282A>C (hg19) ; chr1:g.117147660A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147660A>C , CM000663.2:g.117147660A>C	GRCh38
NC_000001.10:g.117690282A>C , CM000663.1:g.117690282A>C	GRCh37
NC_000001.9:g.117491805A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.847T>G MANE Select	ENSP00000358470.3:p.Ter283Glu
ENST00000328189.7:c.499T>G	ENSP00000328168.3:p.Ter167Glu
ENST00000359008.8:c.856T>G	ENSP00000351899.4:p.Ter286Glu
ENST00000369458.7:c.847T>G	ENSP00000358470.3:p.Ter283Glu
ENST00000539893.5:c.562T>G	ENSP00000444724.1:p.Ter188Glu
NM_001253849.1:c.562T>G	NP_001240778.1:p.Ter188Glu
NM_001253850.1:c.499T>G	NP_001240779.1:p.Ter167Glu
NM_024626.3:c.847T>G	NP_078902.2:p.Ter283Glu
NR_045603.1:n.1042T>G
NR_045604.1:n.746T>G
XM_011542143.1:c.898T>G	XP_011540445.1:p.Ter300Glu
XM_011542144.1:c.901T>G	XP_011540446.1:p.Ter301Glu
XM_011542145.1:c.862T>G	XP_011540447.1:p.Ter288Glu
XM_011542143.2:c.997T>G	XP_011540445.2:p.Ter333Glu
XM_017002335.2:c.862T>G	XP_016857824.1:p.Ter288Glu
NM_024626.4:c.847T>G MANE Select	NP_078902.2:p.Ter283Glu
NR_045603.2:n.1009T>G
NR_045604.2:n.713T>G
NM_001253849.2:c.562T>G	NP_001240778.1:p.Ter188Glu
NM_001253850.2:c.499T>G	NP_001240779.1:p.Ter167Glu