Canonical Allele Identifier: CA341808151

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690324T>G (hg19) ; chr1:g.117147702T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147702T>G , CM000663.2:g.117147702T>G	GRCh38
NC_000001.10:g.117690324T>G , CM000663.1:g.117690324T>G	GRCh37
NC_000001.9:g.117491847T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.805A>C MANE Select	ENSP00000358470.3:p.Ser269Arg
ENST00000328189.7:c.457A>C	ENSP00000328168.3:p.Ser153Arg
ENST00000359008.8:c.814A>C	ENSP00000351899.4:p.Ser272Arg
ENST00000369458.7:c.805A>C	ENSP00000358470.3:p.Ser269Arg
ENST00000539893.5:c.520A>C	ENSP00000444724.1:p.Ser174Arg
NM_001253849.1:c.520A>C	NP_001240778.1:p.Ser174Arg
NM_001253850.1:c.457A>C	NP_001240779.1:p.Ser153Arg
NM_024626.3:c.805A>C	NP_078902.2:p.Ser269Arg
NR_045603.1:n.1000A>C
NR_045604.1:n.704A>C
XM_011542143.1:c.856A>C	XP_011540445.1:p.Ser286Arg
XM_011542144.1:c.859A>C	XP_011540446.1:p.Ser287Arg
XM_011542145.1:c.820A>C	XP_011540447.1:p.Ser274Arg
XM_011542143.2:c.955A>C	XP_011540445.2:p.Ser319Arg
XM_017002335.2:c.820A>C	XP_016857824.1:p.Ser274Arg
NM_024626.4:c.805A>C MANE Select	NP_078902.2:p.Ser269Arg
NR_045603.2:n.967A>C
NR_045604.2:n.671A>C
NM_001253849.2:c.520A>C	NP_001240778.1:p.Ser174Arg
NM_001253850.2:c.457A>C	NP_001240779.1:p.Ser153Arg