Canonical Allele Identifier: CA1191316893

Gene: VTCN1

Linked Data

• dbSNP Id: rs1651584186

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147679del , CM000663.2:g.117147679del	GRCh38
NC_000001.10:g.117690301del , CM000663.1:g.117690301del	GRCh37
NC_000001.9:g.117491824del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.830del MANE Select	ENSP00000358470.3:p.Pro277LeufsTer3
ENST00000328189.7:c.482del	ENSP00000328168.3:p.Pro161LeufsTer3
ENST00000359008.8:c.839del	ENSP00000351899.4:p.Pro280LeufsTer3
ENST00000369458.7:c.830del	ENSP00000358470.3:p.Pro277LeufsTer3
ENST00000539893.5:c.545del	ENSP00000444724.1:p.Pro182LeufsTer3
NM_001253849.1:c.545del	NP_001240778.1:p.Pro182LeufsTer3
NM_001253850.1:c.482del	NP_001240779.1:p.Pro161LeufsTer3
NM_024626.3:c.830del	NP_078902.2:p.Pro277LeufsTer3
NR_045603.1:n.1025del
NR_045604.1:n.729del
XM_011542143.1:c.881del	XP_011540445.1:p.Pro294LeufsTer3
XM_011542144.1:c.884del	XP_011540446.1:p.Pro295LeufsTer3
XM_011542145.1:c.845del	XP_011540447.1:p.Pro282LeufsTer3
XM_011542143.2:c.980del	XP_011540445.2:p.Pro327LeufsTer3
XM_017002335.2:c.845del	XP_016857824.1:p.Pro282LeufsTer3
NM_024626.4:c.830del MANE Select	NP_078902.2:p.Pro277LeufsTer3
NR_045603.2:n.992del
NR_045604.2:n.696del
NM_001253849.2:c.545del	NP_001240778.1:p.Pro182LeufsTer3
NM_001253850.2:c.482del	NP_001240779.1:p.Pro161LeufsTer3