Canonical Allele Identifier: CA341808062

Gene: VTCN1

Linked Data

• gnomAD v4: 1-117147679-G-C
• MyVariant Identifiers: chr1:g.117690301G>C (hg19) ; chr1:g.117147679G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147679G>C , CM000663.2:g.117147679G>C	GRCh38
NC_000001.10:g.117690301G>C , CM000663.1:g.117690301G>C	GRCh37
NC_000001.9:g.117491824G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.828C>G MANE Select	ENSP00000358470.3:p.Ser276Arg
ENST00000328189.7:c.480C>G	ENSP00000328168.3:p.Ser160Arg
ENST00000359008.8:c.837C>G	ENSP00000351899.4:p.Ser279Arg
ENST00000369458.7:c.828C>G	ENSP00000358470.3:p.Ser276Arg
ENST00000539893.5:c.543C>G	ENSP00000444724.1:p.Ser181Arg
NM_001253849.1:c.543C>G	NP_001240778.1:p.Ser181Arg
NM_001253850.1:c.480C>G	NP_001240779.1:p.Ser160Arg
NM_024626.3:c.828C>G	NP_078902.2:p.Ser276Arg
NR_045603.1:n.1023C>G
NR_045604.1:n.727C>G
XM_011542143.1:c.879C>G	XP_011540445.1:p.Ser293Arg
XM_011542144.1:c.882C>G	XP_011540446.1:p.Ser294Arg
XM_011542145.1:c.843C>G	XP_011540447.1:p.Ser281Arg
XM_011542143.2:c.978C>G	XP_011540445.2:p.Ser326Arg
XM_017002335.2:c.843C>G	XP_016857824.1:p.Ser281Arg
NM_024626.4:c.828C>G MANE Select	NP_078902.2:p.Ser276Arg
NR_045603.2:n.990C>G
NR_045604.2:n.694C>G
NM_001253849.2:c.543C>G	NP_001240778.1:p.Ser181Arg
NM_001253850.2:c.480C>G	NP_001240779.1:p.Ser160Arg