Canonical Allele Identifier: CA1191316908

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147736C= , CM000663.2:g.117147736C=	GRCh38
NC_000001.10:g.117690358C= , CM000663.1:g.117690358C=	GRCh37
NC_000001.9:g.117491881C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.771G= MANE Select	ENSP00000358470.3:p.Lys257=
ENST00000328189.7:c.423G=	ENSP00000328168.3:p.Lys141=
ENST00000359008.8:c.780G=	ENSP00000351899.4:p.Lys260=
ENST00000369458.7:c.771G=	ENSP00000358470.3:p.Lys257=
ENST00000539893.5:c.486G=	ENSP00000444724.1:p.Lys162=
NM_001253849.1:c.486G=	NP_001240778.1:p.Lys162=
NM_001253850.1:c.423G=	NP_001240779.1:p.Lys141=
NM_024626.3:c.771G=	NP_078902.2:p.Lys257=
NR_045603.1:n.966G=
NR_045604.1:n.670G=
XM_011542143.1:c.822G=	XP_011540445.1:p.Lys274=
XM_011542144.1:c.825G=	XP_011540446.1:p.Lys275=
XM_011542145.1:c.786G=	XP_011540447.1:p.Lys262=
XM_011542143.2:c.921G=	XP_011540445.2:p.Lys307=
XM_017002335.2:c.786G=	XP_016857824.1:p.Lys262=
NM_024626.4:c.771G= MANE Select	NP_078902.2:p.Lys257=
NR_045603.2:n.933G=
NR_045604.2:n.637G=
NM_001253849.2:c.486G=	NP_001240778.1:p.Lys162=
NM_001253850.2:c.423G=	NP_001240779.1:p.Lys141=