Canonical Allele Identifier: CA1140317160

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117208743C= , CM000663.2:g.117208743C=	GRCh38
NC_000001.10:g.117751365C= , CM000663.1:g.117751365C=	GRCh37
NC_000001.9:g.117552888C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.32+2081G= MANE Select	ENSP00000358470.3:n.32+2081G=
ENST00000328189.7:c.32+2081G=	ENSP00000328168.3:n.32+2081G=
ENST00000369458.7:c.32+2081G=	ENSP00000358470.3:n.32+2081G=
ENST00000430871.3:c.32+2081G=	ENSP00000484316.1:n.32+2081G=
ENST00000463461.5:n.104+2081G=
NM_001253850.1:c.32+2081G=	NP_001240779.1:n.32+2081G=
NM_024626.3:c.32+2081G=	NP_078902.2:n.32+2081G=
NR_045603.1:n.137+2081G=
NR_045604.1:n.137+2081G=
XM_011542144.1:c.87-38572G=	XP_011540446.1:n.87-38572G=
XM_017002335.2:c.-232+2081G=	XP_016857824.1:n.-232+2081G=
NM_024626.4:c.32+2081G= MANE Select	NP_078902.2:n.32+2081G=
NR_045603.2:n.104+2081G=
NR_045604.2:n.104+2081G=
NM_001253850.2:c.32+2081G=	NP_001240779.1:n.32+2081G=