Canonical Allele Identifier: CA341807993

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690281T>A (hg19) ; chr1:g.117147659T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147659T>A , CM000663.2:g.117147659T>A	GRCh38
NC_000001.10:g.117690281T>A , CM000663.1:g.117690281T>A	GRCh37
NC_000001.9:g.117491804T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.848A>T MANE Select	ENSP00000358470.3:p.Ter283Leu
ENST00000328189.7:c.500A>T	ENSP00000328168.3:p.Ter167Leu
ENST00000359008.8:c.857A>T	ENSP00000351899.4:p.Ter286Leu
ENST00000369458.7:c.848A>T	ENSP00000358470.3:p.Ter283Leu
ENST00000539893.5:c.563A>T	ENSP00000444724.1:p.Ter188Leu
NM_001253849.1:c.563A>T	NP_001240778.1:p.Ter188Leu
NM_001253850.1:c.500A>T	NP_001240779.1:p.Ter167Leu
NM_024626.3:c.848A>T	NP_078902.2:p.Ter283Leu
NR_045603.1:n.1043A>T
NR_045604.1:n.747A>T
XM_011542143.1:c.899A>T	XP_011540445.1:p.Ter300Leu
XM_011542144.1:c.902A>T	XP_011540446.1:p.Ter301Leu
XM_011542145.1:c.863A>T	XP_011540447.1:p.Ter288Leu
XM_011542143.2:c.998A>T	XP_011540445.2:p.Ter333Leu
XM_017002335.2:c.863A>T	XP_016857824.1:p.Ter288Leu
NM_024626.4:c.848A>T MANE Select	NP_078902.2:p.Ter283Leu
NR_045603.2:n.1010A>T
NR_045604.2:n.714A>T
NM_001253849.2:c.563A>T	NP_001240778.1:p.Ter188Leu
NM_001253850.2:c.500A>T	NP_001240779.1:p.Ter167Leu