Canonical Allele Identifier: CA341808009

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690285T>A (hg19) ; chr1:g.117147663T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147663T>A , CM000663.2:g.117147663T>A	GRCh38
NC_000001.10:g.117690285T>A , CM000663.1:g.117690285T>A	GRCh37
NC_000001.9:g.117491808T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369458.8:c.844A>T MANE Select	ENSP00000358470.3:p.Lys282Ter
ENST00000328189.7:c.496A>T	ENSP00000328168.3:p.Lys166Ter
ENST00000359008.8:c.853A>T	ENSP00000351899.4:p.Lys285Ter
ENST00000369458.7:c.844A>T	ENSP00000358470.3:p.Lys282Ter
ENST00000539893.5:c.559A>T	ENSP00000444724.1:p.Lys187Ter
NM_001253849.1:c.559A>T	NP_001240778.1:p.Lys187Ter
NM_001253850.1:c.496A>T	NP_001240779.1:p.Lys166Ter
NM_024626.3:c.844A>T	NP_078902.2:p.Lys282Ter
NR_045603.1:n.1039A>T
NR_045604.1:n.743A>T
XM_011542143.1:c.895A>T	XP_011540445.1:p.Lys299Ter
XM_011542144.1:c.898A>T	XP_011540446.1:p.Lys300Ter
XM_011542145.1:c.859A>T	XP_011540447.1:p.Lys287Ter
XM_011542143.2:c.994A>T	XP_011540445.2:p.Lys332Ter
XM_017002335.2:c.859A>T	XP_016857824.1:p.Lys287Ter
NM_024626.4:c.844A>T MANE Select	NP_078902.2:p.Lys282Ter
NR_045603.2:n.1006A>T
NR_045604.2:n.710A>T
NM_001253849.2:c.559A>T	NP_001240778.1:p.Lys187Ter
NM_001253850.2:c.496A>T	NP_001240779.1:p.Lys166Ter