Canonical Allele Identifier: CA341808149

Gene: VTCN1

Linked Data

• dbSNP Id: rs1651585629
• MyVariant Identifiers: chr1:g.117690324T>C (hg19) ; chr1:g.117147702T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.805A>G MANE Select	ENSP00000358470.3:p.Ser269Gly
ENST00000328189.7:c.457A>G	ENSP00000328168.3:p.Ser153Gly
ENST00000359008.8:c.814A>G	ENSP00000351899.4:p.Ser272Gly
ENST00000369458.7:c.805A>G	ENSP00000358470.3:p.Ser269Gly
ENST00000539893.5:c.520A>G	ENSP00000444724.1:p.Ser174Gly
NM_001253849.1:c.520A>G	NP_001240778.1:p.Ser174Gly
NM_001253850.1:c.457A>G	NP_001240779.1:p.Ser153Gly
NM_024626.3:c.805A>G	NP_078902.2:p.Ser269Gly
NR_045603.1:n.1000A>G
NR_045604.1:n.704A>G
XM_011542143.1:c.856A>G	XP_011540445.1:p.Ser286Gly
XM_011542144.1:c.859A>G	XP_011540446.1:p.Ser287Gly
XM_011542145.1:c.820A>G	XP_011540447.1:p.Ser274Gly
XM_011542143.2:c.955A>G	XP_011540445.2:p.Ser319Gly
XM_017002335.2:c.820A>G	XP_016857824.1:p.Ser274Gly
NM_024626.4:c.805A>G MANE Select	NP_078902.2:p.Ser269Gly
NR_045603.2:n.967A>G
NR_045604.2:n.671A>G
NM_001253849.2:c.520A>G	NP_001240778.1:p.Ser174Gly
NM_001253850.2:c.457A>G	NP_001240779.1:p.Ser153Gly