Canonical Allele Identifier: CA1147559645

Gene: VTCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147667C= , CM000663.2:g.117147667C=	GRCh38
NC_000001.10:g.117690289C= , CM000663.1:g.117690289C=	GRCh37
NC_000001.9:g.117491812C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.840G= MANE Select	ENSP00000358470.3:p.Met280=
ENST00000328189.7:c.492G=	ENSP00000328168.3:p.Met164=
ENST00000359008.8:c.849G=	ENSP00000351899.4:p.Met283=
ENST00000369458.7:c.840G=	ENSP00000358470.3:p.Met280=
ENST00000539893.5:c.555G=	ENSP00000444724.1:p.Met185=
NM_001253849.1:c.555G=	NP_001240778.1:p.Met185=
NM_001253850.1:c.492G=	NP_001240779.1:p.Met164=
NM_024626.3:c.840G=	NP_078902.2:p.Met280=
NR_045603.1:n.1035G=
NR_045604.1:n.739G=
XM_011542143.1:c.891G=	XP_011540445.1:p.Met297=
XM_011542144.1:c.894G=	XP_011540446.1:p.Met298=
XM_011542145.1:c.855G=	XP_011540447.1:p.Met285=
XM_011542143.2:c.990G=	XP_011540445.2:p.Met330=
XM_017002335.2:c.855G=	XP_016857824.1:p.Met285=
NM_024626.4:c.840G= MANE Select	NP_078902.2:p.Met280=
NR_045603.2:n.1002G=
NR_045604.2:n.706G=
NM_001253849.2:c.555G=	NP_001240778.1:p.Met185=
NM_001253850.2:c.492G=	NP_001240779.1:p.Met164=