Canonical Allele Identifier: CA419932307

Gene: VTCN1

Linked Data

• gnomAD v4: 1-117147664-T-C
• MyVariant Identifiers: chr1:g.117690286T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147664T>C , CM000663.2:g.117147664T>C	GRCh38
NC_000001.10:g.117690286T>C , CM000663.1:g.117690286T>C	GRCh37
NC_000001.9:g.117491809T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.843A>G MANE Select	ENSP00000358470.3:p.Leu281=
ENST00000328189.7:c.495A>G	ENSP00000328168.3:p.Leu165=
ENST00000359008.8:c.852A>G	ENSP00000351899.4:p.Leu284=
ENST00000369458.7:c.843A>G	ENSP00000358470.3:p.Leu281=
ENST00000539893.5:c.558A>G	ENSP00000444724.1:p.Leu186=
NM_001253849.1:c.558A>G	NP_001240778.1:p.Leu186=
NM_001253850.1:c.495A>G	NP_001240779.1:p.Leu165=
NM_024626.3:c.843A>G	NP_078902.2:p.Leu281=
NR_045603.1:n.1038A>G
NR_045604.1:n.742A>G
XM_011542143.1:c.894A>G	XP_011540445.1:p.Leu298=
XM_011542144.1:c.897A>G	XP_011540446.1:p.Leu299=
XM_011542145.1:c.858A>G	XP_011540447.1:p.Leu286=
XM_011542143.2:c.993A>G	XP_011540445.2:p.Leu331=
XM_017002335.2:c.858A>G	XP_016857824.1:p.Leu286=
NM_024626.4:c.843A>G MANE Select	NP_078902.2:p.Leu281=
NR_045603.2:n.1005A>G
NR_045604.2:n.709A>G
NM_001253849.2:c.558A>G	NP_001240778.1:p.Leu186=
NM_001253850.2:c.495A>G	NP_001240779.1:p.Leu165=