Canonical Allele Identifier: CA1191316902

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147713_117147716delinsAAAG , CM000663.2:g.117147713_117147716delinsAAAG	GRCh38
NC_000001.10:g.117690335_117690338delinsAAAG , CM000663.1:g.117690335_117690338delinsAAAG	GRCh37
NC_000001.9:g.117491858_117491861delinsAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.791_794delinsCTTT MANE Select	ENSP00000358470.3:p.Ser264=
ENST00000328189.7:c.443_446delinsCTTT	ENSP00000328168.3:p.Ser148=
ENST00000359008.8:c.800_803delinsCTTT	ENSP00000351899.4:p.Ser267=
ENST00000369458.7:c.791_794delinsCTTT	ENSP00000358470.3:p.Ser264=
ENST00000539893.5:c.506_509delinsCTTT	ENSP00000444724.1:p.Ser169=
NM_001253849.1:c.506_509delinsCTTT	NP_001240778.1:p.Ser169=
NM_001253850.1:c.443_446delinsCTTT	NP_001240779.1:p.Ser148=
NM_024626.3:c.791_794delinsCTTT	NP_078902.2:p.Ser264=
NR_045603.1:n.986_989delinsCTTT
NR_045604.1:n.690_693delinsCTTT
XM_011542143.1:c.842_845delinsCTTT	XP_011540445.1:p.Ser281=
XM_011542144.1:c.845_848delinsCTTT	XP_011540446.1:p.Ser282=
XM_011542145.1:c.806_809delinsCTTT	XP_011540447.1:p.Ser269=
XM_011542143.2:c.941_944delinsCTTT	XP_011540445.2:p.Ser314=
XM_017002335.2:c.806_809delinsCTTT	XP_016857824.1:p.Ser269=
NM_024626.4:c.791_794delinsCTTT MANE Select	NP_078902.2:p.Ser264=
NR_045603.2:n.953_956delinsCTTT
NR_045604.2:n.657_660delinsCTTT
NM_001253849.2:c.506_509delinsCTTT	NP_001240778.1:p.Ser169=
NM_001253850.2:c.443_446delinsCTTT	NP_001240779.1:p.Ser148=