Canonical Allele Identifier: CA1145609467

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147634_117147638delinsATGCT , CM000663.2:g.117147634_117147638delinsATGCT	GRCh38
NC_000001.10:g.117690256_117690260delinsATGCT , CM000663.1:g.117690256_117690260delinsATGCT	GRCh37
NC_000001.9:g.117491779_117491783delinsATGCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.*20_*24delinsAGCAT MANE Select	ENSP00000358470.3:n.*20_*24delinsAGCAT
ENST00000328189.7:c.*20_*24delinsAGCAT	ENSP00000328168.3:n.*20_*24delinsAGCAT
ENST00000359008.8:c.*20_*24delinsAGCAT	ENSP00000351899.4:n.*20_*24delinsAGCAT
ENST00000369458.7:c.*20_*24delinsAGCAT	ENSP00000358470.3:n.*20_*24delinsAGCAT
ENST00000539893.5:c.*20_*24delinsAGCAT	ENSP00000444724.1:n.*20_*24delinsAGCAT
NM_001253849.1:c.*20_*24delinsAGCAT	NP_001240778.1:n.*20_*24delinsAGCAT
NM_001253850.1:c.*20_*24delinsAGCAT	NP_001240779.1:n.*20_*24delinsAGCAT
NM_024626.3:c.*20_*24delinsAGCAT	NP_078902.2:n.*20_*24delinsAGCAT
NR_045603.1:n.1064_1068delinsAGCAT
NR_045604.1:n.768_772delinsAGCAT
XM_011542143.1:c.*20_*24delinsAGCAT	XP_011540445.1:n.*20_*24delinsAGCAT
XM_011542144.1:c.*20_*24delinsAGCAT	XP_011540446.1:n.*20_*24delinsAGCAT
XM_011542145.1:c.*20_*24delinsAGCAT	XP_011540447.1:n.*20_*24delinsAGCAT
XM_011542143.2:c.*20_*24delinsAGCAT	XP_011540445.2:n.*20_*24delinsAGCAT
XM_017002335.2:c.*20_*24delinsAGCAT	XP_016857824.1:n.*20_*24delinsAGCAT
NM_024626.4:c.*20_*24delinsAGCAT MANE Select	NP_078902.2:n.*20_*24delinsAGCAT
NR_045603.2:n.1031_1035delinsAGCAT
NR_045604.2:n.735_739delinsAGCAT
NM_001253849.2:c.*20_*24delinsAGCAT	NP_001240778.1:n.*20_*24delinsAGCAT
NM_001253850.2:c.*20_*24delinsAGCAT	NP_001240779.1:n.*20_*24delinsAGCAT