Canonical Allele Identifier: CA1191316904

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147725C= , CM000663.2:g.117147725C=	GRCh38
NC_000001.10:g.117690347C= , CM000663.1:g.117690347C=	GRCh37
NC_000001.9:g.117491870C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.782G= MANE Select	ENSP00000358470.3:p.Cys261=
ENST00000328189.7:c.434G=	ENSP00000328168.3:p.Cys145=
ENST00000359008.8:c.791G=	ENSP00000351899.4:p.Cys264=
ENST00000369458.7:c.782G=	ENSP00000358470.3:p.Cys261=
ENST00000539893.5:c.497G=	ENSP00000444724.1:p.Cys166=
NM_001253849.1:c.497G=	NP_001240778.1:p.Cys166=
NM_001253850.1:c.434G=	NP_001240779.1:p.Cys145=
NM_024626.3:c.782G=	NP_078902.2:p.Cys261=
NR_045603.1:n.977G=
NR_045604.1:n.681G=
XM_011542143.1:c.833G=	XP_011540445.1:p.Cys278=
XM_011542144.1:c.836G=	XP_011540446.1:p.Cys279=
XM_011542145.1:c.797G=	XP_011540447.1:p.Cys266=
XM_011542143.2:c.932G=	XP_011540445.2:p.Cys311=
XM_017002335.2:c.797G=	XP_016857824.1:p.Cys266=
NM_024626.4:c.782G= MANE Select	NP_078902.2:p.Cys261=
NR_045603.2:n.944G=
NR_045604.2:n.648G=
NM_001253849.2:c.497G=	NP_001240778.1:p.Cys166=
NM_001253850.2:c.434G=	NP_001240779.1:p.Cys145=