Canonical Allele Identifier: CA341808042

Gene: VTCN1

Linked Data

• gnomAD v4: 1-117147673-G-C
• MyVariant Identifiers: chr1:g.117690295G>C (hg19) ; chr1:g.117147673G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147673G>C , CM000663.2:g.117147673G>C	GRCh38
NC_000001.10:g.117690295G>C , CM000663.1:g.117690295G>C	GRCh37
NC_000001.9:g.117491818G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.834C>G MANE Select	ENSP00000358470.3:p.Tyr278Ter
ENST00000328189.7:c.486C>G	ENSP00000328168.3:p.Tyr162Ter
ENST00000359008.8:c.843C>G	ENSP00000351899.4:p.Tyr281Ter
ENST00000369458.7:c.834C>G	ENSP00000358470.3:p.Tyr278Ter
ENST00000539893.5:c.549C>G	ENSP00000444724.1:p.Tyr183Ter
NM_001253849.1:c.549C>G	NP_001240778.1:p.Tyr183Ter
NM_001253850.1:c.486C>G	NP_001240779.1:p.Tyr162Ter
NM_024626.3:c.834C>G	NP_078902.2:p.Tyr278Ter
NR_045603.1:n.1029C>G
NR_045604.1:n.733C>G
XM_011542143.1:c.885C>G	XP_011540445.1:p.Tyr295Ter
XM_011542144.1:c.888C>G	XP_011540446.1:p.Tyr296Ter
XM_011542145.1:c.849C>G	XP_011540447.1:p.Tyr283Ter
XM_011542143.2:c.984C>G	XP_011540445.2:p.Tyr328Ter
XM_017002335.2:c.849C>G	XP_016857824.1:p.Tyr283Ter
NM_024626.4:c.834C>G MANE Select	NP_078902.2:p.Tyr278Ter
NR_045603.2:n.996C>G
NR_045604.2:n.700C>G
NM_001253849.2:c.549C>G	NP_001240778.1:p.Tyr183Ter
NM_001253850.2:c.486C>G	NP_001240779.1:p.Tyr162Ter