Canonical Allele Identifier: CA1148461963

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147722_117147728delinsACACACA , CM000663.2:g.117147722_117147728delinsACACACA	GRCh38
NC_000001.10:g.117690344_117690350delinsACACACA , CM000663.1:g.117690344_117690350delinsACACACA	GRCh37
NC_000001.9:g.117491867_117491873delinsACACACA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.779_785delinsTGTGTGT MANE Select	ENSP00000358470.3:p.Leu260=
ENST00000328189.7:c.431_437delinsTGTGTGT	ENSP00000328168.3:p.Leu144=
ENST00000359008.8:c.788_794delinsTGTGTGT	ENSP00000351899.4:p.Leu263=
ENST00000369458.7:c.779_785delinsTGTGTGT	ENSP00000358470.3:p.Leu260=
ENST00000539893.5:c.494_500delinsTGTGTGT	ENSP00000444724.1:p.Leu165=
NM_001253849.1:c.494_500delinsTGTGTGT	NP_001240778.1:p.Leu165=
NM_001253850.1:c.431_437delinsTGTGTGT	NP_001240779.1:p.Leu144=
NM_024626.3:c.779_785delinsTGTGTGT	NP_078902.2:p.Leu260=
NR_045603.1:n.974_980delinsTGTGTGT
NR_045604.1:n.678_684delinsTGTGTGT
XM_011542143.1:c.830_836delinsTGTGTGT	XP_011540445.1:p.Leu277=
XM_011542144.1:c.833_839delinsTGTGTGT	XP_011540446.1:p.Leu278=
XM_011542145.1:c.794_800delinsTGTGTGT	XP_011540447.1:p.Leu265=
XM_011542143.2:c.929_935delinsTGTGTGT	XP_011540445.2:p.Leu310=
XM_017002335.2:c.794_800delinsTGTGTGT	XP_016857824.1:p.Leu265=
NM_024626.4:c.779_785delinsTGTGTGT MANE Select	NP_078902.2:p.Leu260=
NR_045603.2:n.941_947delinsTGTGTGT
NR_045604.2:n.645_651delinsTGTGTGT
NM_001253849.2:c.494_500delinsTGTGTGT	NP_001240778.1:p.Leu165=
NM_001253850.2:c.431_437delinsTGTGTGT	NP_001240779.1:p.Leu144=