Canonical Allele Identifier: CA1191316905

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147731G= , CM000663.2:g.117147731G=	GRCh38
NC_000001.10:g.117690353G= , CM000663.1:g.117690353G=	GRCh37
NC_000001.9:g.117491876G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.776C= MANE Select	ENSP00000358470.3:p.Ser259=
ENST00000328189.7:c.428C=	ENSP00000328168.3:p.Ser143=
ENST00000359008.8:c.785C=	ENSP00000351899.4:p.Ser262=
ENST00000369458.7:c.776C=	ENSP00000358470.3:p.Ser259=
ENST00000539893.5:c.491C=	ENSP00000444724.1:p.Ser164=
NM_001253849.1:c.491C=	NP_001240778.1:p.Ser164=
NM_001253850.1:c.428C=	NP_001240779.1:p.Ser143=
NM_024626.3:c.776C=	NP_078902.2:p.Ser259=
NR_045603.1:n.971C=
NR_045604.1:n.675C=
XM_011542143.1:c.827C=	XP_011540445.1:p.Ser276=
XM_011542144.1:c.830C=	XP_011540446.1:p.Ser277=
XM_011542145.1:c.791C=	XP_011540447.1:p.Ser264=
XM_011542143.2:c.926C=	XP_011540445.2:p.Ser309=
XM_017002335.2:c.791C=	XP_016857824.1:p.Ser264=
NM_024626.4:c.776C= MANE Select	NP_078902.2:p.Ser259=
NR_045603.2:n.938C=
NR_045604.2:n.642C=
NM_001253849.2:c.491C=	NP_001240778.1:p.Ser164=
NM_001253850.2:c.428C=	NP_001240779.1:p.Ser143=