Canonical Allele Identifier: CA1143872163

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147715A= , CM000663.2:g.117147715A=	GRCh38
NC_000001.10:g.117690337A= , CM000663.1:g.117690337A=	GRCh37
NC_000001.9:g.117491860A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.792T= MANE Select	ENSP00000358470.3:p.Ser264=
ENST00000328189.7:c.444T=	ENSP00000328168.3:p.Ser148=
ENST00000359008.8:c.801T=	ENSP00000351899.4:p.Ser267=
ENST00000369458.7:c.792T=	ENSP00000358470.3:p.Ser264=
ENST00000539893.5:c.507T=	ENSP00000444724.1:p.Ser169=
NM_001253849.1:c.507T=	NP_001240778.1:p.Ser169=
NM_001253850.1:c.444T=	NP_001240779.1:p.Ser148=
NM_024626.3:c.792T=	NP_078902.2:p.Ser264=
NR_045603.1:n.987T=
NR_045604.1:n.691T=
XM_011542143.1:c.843T=	XP_011540445.1:p.Ser281=
XM_011542144.1:c.846T=	XP_011540446.1:p.Ser282=
XM_011542145.1:c.807T=	XP_011540447.1:p.Ser269=
XM_011542143.2:c.942T=	XP_011540445.2:p.Ser314=
XM_017002335.2:c.807T=	XP_016857824.1:p.Ser269=
NM_024626.4:c.792T= MANE Select	NP_078902.2:p.Ser264=
NR_045603.2:n.954T=
NR_045604.2:n.658T=
NM_001253849.2:c.507T=	NP_001240778.1:p.Ser169=
NM_001253850.2:c.444T=	NP_001240779.1:p.Ser148=