Canonical Allele Identifier: CA341808029

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690290A>T (hg19) ; chr1:g.117147668A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147668A>T , CM000663.2:g.117147668A>T	GRCh38
NC_000001.10:g.117690290A>T , CM000663.1:g.117690290A>T	GRCh37
NC_000001.9:g.117491813A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.839T>A MANE Select	ENSP00000358470.3:p.Met280Lys
ENST00000328189.7:c.491T>A	ENSP00000328168.3:p.Met164Lys
ENST00000359008.8:c.848T>A	ENSP00000351899.4:p.Met283Lys
ENST00000369458.7:c.839T>A	ENSP00000358470.3:p.Met280Lys
ENST00000539893.5:c.554T>A	ENSP00000444724.1:p.Met185Lys
NM_001253849.1:c.554T>A	NP_001240778.1:p.Met185Lys
NM_001253850.1:c.491T>A	NP_001240779.1:p.Met164Lys
NM_024626.3:c.839T>A	NP_078902.2:p.Met280Lys
NR_045603.1:n.1034T>A
NR_045604.1:n.738T>A
XM_011542143.1:c.890T>A	XP_011540445.1:p.Met297Lys
XM_011542144.1:c.893T>A	XP_011540446.1:p.Met298Lys
XM_011542145.1:c.854T>A	XP_011540447.1:p.Met285Lys
XM_011542143.2:c.989T>A	XP_011540445.2:p.Met330Lys
XM_017002335.2:c.854T>A	XP_016857824.1:p.Met285Lys
NM_024626.4:c.839T>A MANE Select	NP_078902.2:p.Met280Lys
NR_045603.2:n.1001T>A
NR_045604.2:n.705T>A
NM_001253849.2:c.554T>A	NP_001240778.1:p.Met185Lys
NM_001253850.2:c.491T>A	NP_001240779.1:p.Met164Lys