Canonical Allele Identifier: CA341808141

Gene: VTCN1

Linked Data

• dbSNP Id: rs756445973
• MyVariant Identifiers: chr1:g.117690323C>T (hg19) ; chr1:g.117147701C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147701C>T , CM000663.2:g.117147701C>T	GRCh38
NC_000001.10:g.117690323C>T , CM000663.1:g.117690323C>T	GRCh37
NC_000001.9:g.117491846C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.806G>A MANE Select	ENSP00000358470.3:p.Ser269Asn
ENST00000328189.7:c.458G>A	ENSP00000328168.3:p.Ser153Asn
ENST00000359008.8:c.815G>A	ENSP00000351899.4:p.Ser272Asn
ENST00000369458.7:c.806G>A	ENSP00000358470.3:p.Ser269Asn
ENST00000539893.5:c.521G>A	ENSP00000444724.1:p.Ser174Asn
NM_001253849.1:c.521G>A	NP_001240778.1:p.Ser174Asn
NM_001253850.1:c.458G>A	NP_001240779.1:p.Ser153Asn
NM_024626.3:c.806G>A	NP_078902.2:p.Ser269Asn
NR_045603.1:n.1001G>A
NR_045604.1:n.705G>A
XM_011542143.1:c.857G>A	XP_011540445.1:p.Ser286Asn
XM_011542144.1:c.860G>A	XP_011540446.1:p.Ser287Asn
XM_011542145.1:c.821G>A	XP_011540447.1:p.Ser274Asn
XM_011542143.2:c.956G>A	XP_011540445.2:p.Ser319Asn
XM_017002335.2:c.821G>A	XP_016857824.1:p.Ser274Asn
NM_024626.4:c.806G>A MANE Select	NP_078902.2:p.Ser269Asn
NR_045603.2:n.968G>A
NR_045604.2:n.672G>A
NM_001253849.2:c.521G>A	NP_001240778.1:p.Ser174Asn
NM_001253850.2:c.458G>A	NP_001240779.1:p.Ser153Asn