Canonical Allele Identifier: CA419932383

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690340A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147718A>C , CM000663.2:g.117147718A>C	GRCh38
NC_000001.10:g.117690340A>C , CM000663.1:g.117690340A>C	GRCh37
NC_000001.9:g.117491863A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.789T>G MANE Select	ENSP00000358470.3:p.Ser263=
ENST00000328189.7:c.441T>G	ENSP00000328168.3:p.Ser147=
ENST00000359008.8:c.798T>G	ENSP00000351899.4:p.Ser266=
ENST00000369458.7:c.789T>G	ENSP00000358470.3:p.Ser263=
ENST00000539893.5:c.504T>G	ENSP00000444724.1:p.Ser168=
NM_001253849.1:c.504T>G	NP_001240778.1:p.Ser168=
NM_001253850.1:c.441T>G	NP_001240779.1:p.Ser147=
NM_024626.3:c.789T>G	NP_078902.2:p.Ser263=
NR_045603.1:n.984T>G
NR_045604.1:n.688T>G
XM_011542143.1:c.840T>G	XP_011540445.1:p.Ser280=
XM_011542144.1:c.843T>G	XP_011540446.1:p.Ser281=
XM_011542145.1:c.804T>G	XP_011540447.1:p.Ser268=
XM_011542143.2:c.939T>G	XP_011540445.2:p.Ser313=
XM_017002335.2:c.804T>G	XP_016857824.1:p.Ser268=
NM_024626.4:c.789T>G MANE Select	NP_078902.2:p.Ser263=
NR_045603.2:n.951T>G
NR_045604.2:n.655T>G
NM_001253849.2:c.504T>G	NP_001240778.1:p.Ser168=
NM_001253850.2:c.441T>G	NP_001240779.1:p.Ser147=