Canonical Allele Identifier: CA1191316901

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147702T= , CM000663.2:g.117147702T=	GRCh38
NC_000001.10:g.117690324T= , CM000663.1:g.117690324T=	GRCh37
NC_000001.9:g.117491847T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.805A= MANE Select	ENSP00000358470.3:p.Ser269=
ENST00000328189.7:c.457A=	ENSP00000328168.3:p.Ser153=
ENST00000359008.8:c.814A=	ENSP00000351899.4:p.Ser272=
ENST00000369458.7:c.805A=	ENSP00000358470.3:p.Ser269=
ENST00000539893.5:c.520A=	ENSP00000444724.1:p.Ser174=
NM_001253849.1:c.520A=	NP_001240778.1:p.Ser174=
NM_001253850.1:c.457A=	NP_001240779.1:p.Ser153=
NM_024626.3:c.805A=	NP_078902.2:p.Ser269=
NR_045603.1:n.1000A=
NR_045604.1:n.704A=
XM_011542143.1:c.856A=	XP_011540445.1:p.Ser286=
XM_011542144.1:c.859A=	XP_011540446.1:p.Ser287=
XM_011542145.1:c.820A=	XP_011540447.1:p.Ser274=
XM_011542143.2:c.955A=	XP_011540445.2:p.Ser319=
XM_017002335.2:c.820A=	XP_016857824.1:p.Ser274=
NM_024626.4:c.805A= MANE Select	NP_078902.2:p.Ser269=
NR_045603.2:n.967A=
NR_045604.2:n.671A=
NM_001253849.2:c.520A=	NP_001240778.1:p.Ser174=
NM_001253850.2:c.457A=	NP_001240779.1:p.Ser153=