Canonical Allele Identifier: CA341808087

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690308G>C (hg19) ; chr1:g.117147686G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147686G>C , CM000663.2:g.117147686G>C	GRCh38
NC_000001.10:g.117690308G>C , CM000663.1:g.117690308G>C	GRCh37
NC_000001.9:g.117491831G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.821C>G MANE Select	ENSP00000358470.3:p.Pro274Arg
ENST00000328189.7:c.473C>G	ENSP00000328168.3:p.Pro158Arg
ENST00000359008.8:c.830C>G	ENSP00000351899.4:p.Pro277Arg
ENST00000369458.7:c.821C>G	ENSP00000358470.3:p.Pro274Arg
ENST00000539893.5:c.536C>G	ENSP00000444724.1:p.Pro179Arg
NM_001253849.1:c.536C>G	NP_001240778.1:p.Pro179Arg
NM_001253850.1:c.473C>G	NP_001240779.1:p.Pro158Arg
NM_024626.3:c.821C>G	NP_078902.2:p.Pro274Arg
NR_045603.1:n.1016C>G
NR_045604.1:n.720C>G
XM_011542143.1:c.872C>G	XP_011540445.1:p.Pro291Arg
XM_011542144.1:c.875C>G	XP_011540446.1:p.Pro292Arg
XM_011542145.1:c.836C>G	XP_011540447.1:p.Pro279Arg
XM_011542143.2:c.971C>G	XP_011540445.2:p.Pro324Arg
XM_017002335.2:c.836C>G	XP_016857824.1:p.Pro279Arg
NM_024626.4:c.821C>G MANE Select	NP_078902.2:p.Pro274Arg
NR_045603.2:n.983C>G
NR_045604.2:n.687C>G
NM_001253849.2:c.536C>G	NP_001240778.1:p.Pro179Arg
NM_001253850.2:c.473C>G	NP_001240779.1:p.Pro158Arg