Canonical Allele Identifier: CA1191316899

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147696C= , CM000663.2:g.117147696C=	GRCh38
NC_000001.10:g.117690318C= , CM000663.1:g.117690318C=	GRCh37
NC_000001.9:g.117491841C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.811G= MANE Select	ENSP00000358470.3:p.Ala271=
ENST00000328189.7:c.463G=	ENSP00000328168.3:p.Ala155=
ENST00000359008.8:c.820G=	ENSP00000351899.4:p.Ala274=
ENST00000369458.7:c.811G=	ENSP00000358470.3:p.Ala271=
ENST00000539893.5:c.526G=	ENSP00000444724.1:p.Ala176=
NM_001253849.1:c.526G=	NP_001240778.1:p.Ala176=
NM_001253850.1:c.463G=	NP_001240779.1:p.Ala155=
NM_024626.3:c.811G=	NP_078902.2:p.Ala271=
NR_045603.1:n.1006G=
NR_045604.1:n.710G=
XM_011542143.1:c.862G=	XP_011540445.1:p.Ala288=
XM_011542144.1:c.865G=	XP_011540446.1:p.Ala289=
XM_011542145.1:c.826G=	XP_011540447.1:p.Ala276=
XM_011542143.2:c.961G=	XP_011540445.2:p.Ala321=
XM_017002335.2:c.826G=	XP_016857824.1:p.Ala276=
NM_024626.4:c.811G= MANE Select	NP_078902.2:p.Ala271=
NR_045603.2:n.973G=
NR_045604.2:n.677G=
NM_001253849.2:c.526G=	NP_001240778.1:p.Ala176=
NM_001253850.2:c.463G=	NP_001240779.1:p.Ala155=