Canonical Allele Identifier: CA341808288

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690359T>A (hg19) ; chr1:g.117147737T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147737T>A , CM000663.2:g.117147737T>A	GRCh38
NC_000001.10:g.117690359T>A , CM000663.1:g.117690359T>A	GRCh37
NC_000001.9:g.117491882T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.770A>T MANE Select	ENSP00000358470.3:p.Lys257Met
ENST00000328189.7:c.422A>T	ENSP00000328168.3:p.Lys141Met
ENST00000359008.8:c.779A>T	ENSP00000351899.4:p.Lys260Met
ENST00000369458.7:c.770A>T	ENSP00000358470.3:p.Lys257Met
ENST00000539893.5:c.485A>T	ENSP00000444724.1:p.Lys162Met
NM_001253849.1:c.485A>T	NP_001240778.1:p.Lys162Met
NM_001253850.1:c.422A>T	NP_001240779.1:p.Lys141Met
NM_024626.3:c.770A>T	NP_078902.2:p.Lys257Met
NR_045603.1:n.965A>T
NR_045604.1:n.669A>T
XM_011542143.1:c.821A>T	XP_011540445.1:p.Lys274Met
XM_011542144.1:c.824A>T	XP_011540446.1:p.Lys275Met
XM_011542145.1:c.785A>T	XP_011540447.1:p.Lys262Met
XM_011542143.2:c.920A>T	XP_011540445.2:p.Lys307Met
XM_017002335.2:c.785A>T	XP_016857824.1:p.Lys262Met
NM_024626.4:c.770A>T MANE Select	NP_078902.2:p.Lys257Met
NR_045603.2:n.932A>T
NR_045604.2:n.636A>T
NM_001253849.2:c.485A>T	NP_001240778.1:p.Lys162Met
NM_001253850.2:c.422A>T	NP_001240779.1:p.Lys141Met