Canonical Allele Identifier: CA341808249

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690347C>G (hg19) ; chr1:g.117147725C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147725C>G , CM000663.2:g.117147725C>G	GRCh38
NC_000001.10:g.117690347C>G , CM000663.1:g.117690347C>G	GRCh37
NC_000001.9:g.117491870C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.782G>C MANE Select	ENSP00000358470.3:p.Cys261Ser
ENST00000328189.7:c.434G>C	ENSP00000328168.3:p.Cys145Ser
ENST00000359008.8:c.791G>C	ENSP00000351899.4:p.Cys264Ser
ENST00000369458.7:c.782G>C	ENSP00000358470.3:p.Cys261Ser
ENST00000539893.5:c.497G>C	ENSP00000444724.1:p.Cys166Ser
NM_001253849.1:c.497G>C	NP_001240778.1:p.Cys166Ser
NM_001253850.1:c.434G>C	NP_001240779.1:p.Cys145Ser
NM_024626.3:c.782G>C	NP_078902.2:p.Cys261Ser
NR_045603.1:n.977G>C
NR_045604.1:n.681G>C
XM_011542143.1:c.833G>C	XP_011540445.1:p.Cys278Ser
XM_011542144.1:c.836G>C	XP_011540446.1:p.Cys279Ser
XM_011542145.1:c.797G>C	XP_011540447.1:p.Cys266Ser
XM_011542143.2:c.932G>C	XP_011540445.2:p.Cys311Ser
XM_017002335.2:c.797G>C	XP_016857824.1:p.Cys266Ser
NM_024626.4:c.782G>C MANE Select	NP_078902.2:p.Cys261Ser
NR_045603.2:n.944G>C
NR_045604.2:n.648G>C
NM_001253849.2:c.497G>C	NP_001240778.1:p.Cys166Ser
NM_001253850.2:c.434G>C	NP_001240779.1:p.Cys145Ser