Canonical Allele Identifier: CA2647331101

Gene: VTCN1

Linked Data

• gnomAD v4: 1-117147667-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147667_117147668insT , CM000663.2:g.117147667_117147668insT	GRCh38
NC_000001.10:g.117690289_117690290insT , CM000663.1:g.117690289_117690290insT	GRCh37
NC_000001.9:g.117491812_117491813insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.839_840insA MANE Select	ENSP00000358470.3:p.Met280IlefsTer?
ENST00000328189.7:c.491_492insA	ENSP00000328168.3:p.Met164IlefsTer?
ENST00000359008.8:c.848_849insA	ENSP00000351899.4:p.Met283IlefsTer?
ENST00000369458.7:c.839_840insA	ENSP00000358470.3:p.Met280IlefsTer?
ENST00000539893.5:c.554_555insA	ENSP00000444724.1:p.Met185IlefsTer?
NM_001253849.1:c.554_555insA	NP_001240778.1:p.Met185IlefsTer?
NM_001253850.1:c.491_492insA	NP_001240779.1:p.Met164IlefsTer?
NM_024626.3:c.839_840insA	NP_078902.2:p.Met280IlefsTer?
NR_045603.1:n.1034_1035insA
NR_045604.1:n.738_739insA
XM_011542143.1:c.890_891insA	XP_011540445.1:p.Met297IlefsTer?
XM_011542144.1:c.893_894insA	XP_011540446.1:p.Met298IlefsTer?
XM_011542145.1:c.854_855insA	XP_011540447.1:p.Met285IlefsTer?
XM_011542143.2:c.989_990insA	XP_011540445.2:p.Met330IlefsTer?
XM_017002335.2:c.854_855insA	XP_016857824.1:p.Met285IlefsTer?
NM_024626.4:c.839_840insA MANE Select	NP_078902.2:p.Met280IlefsTer?
NR_045603.2:n.1001_1002insA
NR_045604.2:n.705_706insA
NM_001253849.2:c.554_555insA	NP_001240778.1:p.Met185IlefsTer?
NM_001253850.2:c.491_492insA	NP_001240779.1:p.Met164IlefsTer?