Canonical Allele Identifier: CA1191316892

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147676_117147677delinsAG , CM000663.2:g.117147676_117147677delinsAG	GRCh38
NC_000001.10:g.117690298_117690299delinsAG , CM000663.1:g.117690298_117690299delinsAG	GRCh37
NC_000001.9:g.117491821_117491822delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.830_831delinsCT MANE Select	ENSP00000358470.3:p.Pro277=
ENST00000328189.7:c.482_483delinsCT	ENSP00000328168.3:p.Pro161=
ENST00000359008.8:c.839_840delinsCT	ENSP00000351899.4:p.Pro280=
ENST00000369458.7:c.830_831delinsCT	ENSP00000358470.3:p.Pro277=
ENST00000539893.5:c.545_546delinsCT	ENSP00000444724.1:p.Pro182=
NM_001253849.1:c.545_546delinsCT	NP_001240778.1:p.Pro182=
NM_001253850.1:c.482_483delinsCT	NP_001240779.1:p.Pro161=
NM_024626.3:c.830_831delinsCT	NP_078902.2:p.Pro277=
NR_045603.1:n.1025_1026delinsCT
NR_045604.1:n.729_730delinsCT
XM_011542143.1:c.881_882delinsCT	XP_011540445.1:p.Pro294=
XM_011542144.1:c.884_885delinsCT	XP_011540446.1:p.Pro295=
XM_011542145.1:c.845_846delinsCT	XP_011540447.1:p.Pro282=
XM_011542143.2:c.980_981delinsCT	XP_011540445.2:p.Pro327=
XM_017002335.2:c.845_846delinsCT	XP_016857824.1:p.Pro282=
NM_024626.4:c.830_831delinsCT MANE Select	NP_078902.2:p.Pro277=
NR_045603.2:n.992_993delinsCT
NR_045604.2:n.696_697delinsCT
NM_001253849.2:c.545_546delinsCT	NP_001240778.1:p.Pro182=
NM_001253850.2:c.482_483delinsCT	NP_001240779.1:p.Pro161=