Canonical Allele Identifier: CA341808047

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690296T>C (hg19) ; chr1:g.117147674T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147674T>C , CM000663.2:g.117147674T>C	GRCh38
NC_000001.10:g.117690296T>C , CM000663.1:g.117690296T>C	GRCh37
NC_000001.9:g.117491819T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.833A>G MANE Select	ENSP00000358470.3:p.Tyr278Cys
ENST00000328189.7:c.485A>G	ENSP00000328168.3:p.Tyr162Cys
ENST00000359008.8:c.842A>G	ENSP00000351899.4:p.Tyr281Cys
ENST00000369458.7:c.833A>G	ENSP00000358470.3:p.Tyr278Cys
ENST00000539893.5:c.548A>G	ENSP00000444724.1:p.Tyr183Cys
NM_001253849.1:c.548A>G	NP_001240778.1:p.Tyr183Cys
NM_001253850.1:c.485A>G	NP_001240779.1:p.Tyr162Cys
NM_024626.3:c.833A>G	NP_078902.2:p.Tyr278Cys
NR_045603.1:n.1028A>G
NR_045604.1:n.732A>G
XM_011542143.1:c.884A>G	XP_011540445.1:p.Tyr295Cys
XM_011542144.1:c.887A>G	XP_011540446.1:p.Tyr296Cys
XM_011542145.1:c.848A>G	XP_011540447.1:p.Tyr283Cys
XM_011542143.2:c.983A>G	XP_011540445.2:p.Tyr328Cys
XM_017002335.2:c.848A>G	XP_016857824.1:p.Tyr283Cys
NM_024626.4:c.833A>G MANE Select	NP_078902.2:p.Tyr278Cys
NR_045603.2:n.995A>G
NR_045604.2:n.699A>G
NM_001253849.2:c.548A>G	NP_001240778.1:p.Tyr183Cys
NM_001253850.2:c.485A>G	NP_001240779.1:p.Tyr162Cys