Canonical Allele Identifier: CA341808086

Gene: VTCN1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.821C>A MANE Select	ENSP00000358470.3:p.Pro274His
ENST00000328189.7:c.473C>A	ENSP00000328168.3:p.Pro158His
ENST00000359008.8:c.830C>A	ENSP00000351899.4:p.Pro277His
ENST00000369458.7:c.821C>A	ENSP00000358470.3:p.Pro274His
ENST00000539893.5:c.536C>A	ENSP00000444724.1:p.Pro179His
NM_001253849.1:c.536C>A	NP_001240778.1:p.Pro179His
NM_001253850.1:c.473C>A	NP_001240779.1:p.Pro158His
NM_024626.3:c.821C>A	NP_078902.2:p.Pro274His
NR_045603.1:n.1016C>A
NR_045604.1:n.720C>A
XM_011542143.1:c.872C>A	XP_011540445.1:p.Pro291His
XM_011542144.1:c.875C>A	XP_011540446.1:p.Pro292His
XM_011542145.1:c.836C>A	XP_011540447.1:p.Pro279His
XM_011542143.2:c.971C>A	XP_011540445.2:p.Pro324His
XM_017002335.2:c.836C>A	XP_016857824.1:p.Pro279His
NM_024626.4:c.821C>A MANE Select	NP_078902.2:p.Pro274His
NR_045603.2:n.983C>A
NR_045604.2:n.687C>A
NM_001253849.2:c.536C>A	NP_001240778.1:p.Pro179His
NM_001253850.2:c.473C>A	NP_001240779.1:p.Pro158His