Canonical Allele Identifier: CA1191316873

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147636G= , CM000663.2:g.117147636G=	GRCh38
NC_000001.10:g.117690258G= , CM000663.1:g.117690258G=	GRCh37
NC_000001.9:g.117491781G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.*22C= MANE Select	ENSP00000358470.3:n.*22C=
ENST00000328189.7:c.*22C=	ENSP00000328168.3:n.*22C=
ENST00000359008.8:c.*22C=	ENSP00000351899.4:n.*22C=
ENST00000369458.7:c.*22C=	ENSP00000358470.3:n.*22C=
ENST00000539893.5:c.*22C=	ENSP00000444724.1:n.*22C=
NM_001253849.1:c.*22C=	NP_001240778.1:n.*22C=
NM_001253850.1:c.*22C=	NP_001240779.1:n.*22C=
NM_024626.3:c.*22C=	NP_078902.2:n.*22C=
NR_045603.1:n.1066C=
NR_045604.1:n.770C=
XM_011542143.1:c.*22C=	XP_011540445.1:n.*22C=
XM_011542144.1:c.*22C=	XP_011540446.1:n.*22C=
XM_011542145.1:c.*22C=	XP_011540447.1:n.*22C=
XM_011542143.2:c.*22C=	XP_011540445.2:n.*22C=
XM_017002335.2:c.*22C=	XP_016857824.1:n.*22C=
NM_024626.4:c.*22C= MANE Select	NP_078902.2:n.*22C=
NR_045603.2:n.1033C=
NR_045604.2:n.737C=
NM_001253849.2:c.*22C=	NP_001240778.1:n.*22C=
NM_001253850.2:c.*22C=	NP_001240779.1:n.*22C=