Canonical Allele Identifier: CA341808292

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690360T>C (hg19) ; chr1:g.117147738T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147738T>C , CM000663.2:g.117147738T>C	GRCh38
NC_000001.10:g.117690360T>C , CM000663.1:g.117690360T>C	GRCh37
NC_000001.9:g.117491883T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.769A>G MANE Select	ENSP00000358470.3:p.Lys257Glu
ENST00000328189.7:c.421A>G	ENSP00000328168.3:p.Lys141Glu
ENST00000359008.8:c.778A>G	ENSP00000351899.4:p.Lys260Glu
ENST00000369458.7:c.769A>G	ENSP00000358470.3:p.Lys257Glu
ENST00000539893.5:c.484A>G	ENSP00000444724.1:p.Lys162Glu
NM_001253849.1:c.484A>G	NP_001240778.1:p.Lys162Glu
NM_001253850.1:c.421A>G	NP_001240779.1:p.Lys141Glu
NM_024626.3:c.769A>G	NP_078902.2:p.Lys257Glu
NR_045603.1:n.964A>G
NR_045604.1:n.668A>G
XM_011542143.1:c.820A>G	XP_011540445.1:p.Lys274Glu
XM_011542144.1:c.823A>G	XP_011540446.1:p.Lys275Glu
XM_011542145.1:c.784A>G	XP_011540447.1:p.Lys262Glu
XM_011542143.2:c.919A>G	XP_011540445.2:p.Lys307Glu
XM_017002335.2:c.784A>G	XP_016857824.1:p.Lys262Glu
NM_024626.4:c.769A>G MANE Select	NP_078902.2:p.Lys257Glu
NR_045603.2:n.931A>G
NR_045604.2:n.635A>G
NM_001253849.2:c.484A>G	NP_001240778.1:p.Lys162Glu
NM_001253850.2:c.421A>G	NP_001240779.1:p.Lys141Glu