Canonical Allele Identifier: CA1191316895

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147679G= , CM000663.2:g.117147679G=	GRCh38
NC_000001.10:g.117690301G= , CM000663.1:g.117690301G=	GRCh37
NC_000001.9:g.117491824G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.828C= MANE Select	ENSP00000358470.3:p.Ser276=
ENST00000328189.7:c.480C=	ENSP00000328168.3:p.Ser160=
ENST00000359008.8:c.837C=	ENSP00000351899.4:p.Ser279=
ENST00000369458.7:c.828C=	ENSP00000358470.3:p.Ser276=
ENST00000539893.5:c.543C=	ENSP00000444724.1:p.Ser181=
NM_001253849.1:c.543C=	NP_001240778.1:p.Ser181=
NM_001253850.1:c.480C=	NP_001240779.1:p.Ser160=
NM_024626.3:c.828C=	NP_078902.2:p.Ser276=
NR_045603.1:n.1023C=
NR_045604.1:n.727C=
XM_011542143.1:c.879C=	XP_011540445.1:p.Ser293=
XM_011542144.1:c.882C=	XP_011540446.1:p.Ser294=
XM_011542145.1:c.843C=	XP_011540447.1:p.Ser281=
XM_011542143.2:c.978C=	XP_011540445.2:p.Ser326=
XM_017002335.2:c.843C=	XP_016857824.1:p.Ser281=
NM_024626.4:c.828C= MANE Select	NP_078902.2:p.Ser276=
NR_045603.2:n.990C=
NR_045604.2:n.694C=
NM_001253849.2:c.543C=	NP_001240778.1:p.Ser181=
NM_001253850.2:c.480C=	NP_001240779.1:p.Ser160=