Canonical Allele Identifier: CA1191316891

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147673G= , CM000663.2:g.117147673G=	GRCh38
NC_000001.10:g.117690295G= , CM000663.1:g.117690295G=	GRCh37
NC_000001.9:g.117491818G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.834C= MANE Select	ENSP00000358470.3:p.Tyr278=
ENST00000328189.7:c.486C=	ENSP00000328168.3:p.Tyr162=
ENST00000359008.8:c.843C=	ENSP00000351899.4:p.Tyr281=
ENST00000369458.7:c.834C=	ENSP00000358470.3:p.Tyr278=
ENST00000539893.5:c.549C=	ENSP00000444724.1:p.Tyr183=
NM_001253849.1:c.549C=	NP_001240778.1:p.Tyr183=
NM_001253850.1:c.486C=	NP_001240779.1:p.Tyr162=
NM_024626.3:c.834C=	NP_078902.2:p.Tyr278=
NR_045603.1:n.1029C=
NR_045604.1:n.733C=
XM_011542143.1:c.885C=	XP_011540445.1:p.Tyr295=
XM_011542144.1:c.888C=	XP_011540446.1:p.Tyr296=
XM_011542145.1:c.849C=	XP_011540447.1:p.Tyr283=
XM_011542143.2:c.984C=	XP_011540445.2:p.Tyr328=
XM_017002335.2:c.849C=	XP_016857824.1:p.Tyr283=
NM_024626.4:c.834C= MANE Select	NP_078902.2:p.Tyr278=
NR_045603.2:n.996C=
NR_045604.2:n.700C=
NM_001253849.2:c.549C=	NP_001240778.1:p.Tyr183=
NM_001253850.2:c.486C=	NP_001240779.1:p.Tyr162=