Canonical Allele Identifier: CA341807994

Gene: VTCN1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.848A>C MANE Select	ENSP00000358470.3:p.Ter283Ser
ENST00000328189.7:c.500A>C	ENSP00000328168.3:p.Ter167Ser
ENST00000359008.8:c.857A>C	ENSP00000351899.4:p.Ter286Ser
ENST00000369458.7:c.848A>C	ENSP00000358470.3:p.Ter283Ser
ENST00000539893.5:c.563A>C	ENSP00000444724.1:p.Ter188Ser
NM_001253849.1:c.563A>C	NP_001240778.1:p.Ter188Ser
NM_001253850.1:c.500A>C	NP_001240779.1:p.Ter167Ser
NM_024626.3:c.848A>C	NP_078902.2:p.Ter283Ser
NR_045603.1:n.1043A>C
NR_045604.1:n.747A>C
XM_011542143.1:c.899A>C	XP_011540445.1:p.Ter300Ser
XM_011542144.1:c.902A>C	XP_011540446.1:p.Ter301Ser
XM_011542145.1:c.863A>C	XP_011540447.1:p.Ter288Ser
XM_011542143.2:c.998A>C	XP_011540445.2:p.Ter333Ser
XM_017002335.2:c.863A>C	XP_016857824.1:p.Ter288Ser
NM_024626.4:c.848A>C MANE Select	NP_078902.2:p.Ter283Ser
NR_045603.2:n.1010A>C
NR_045604.2:n.714A>C
NM_001253849.2:c.563A>C	NP_001240778.1:p.Ter188Ser
NM_001253850.2:c.500A>C	NP_001240779.1:p.Ter167Ser