Canonical Allele Identifier: CA341808045

Gene: VTCN1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.833A>T MANE Select	ENSP00000358470.3:p.Tyr278Phe
ENST00000328189.7:c.485A>T	ENSP00000328168.3:p.Tyr162Phe
ENST00000359008.8:c.842A>T	ENSP00000351899.4:p.Tyr281Phe
ENST00000369458.7:c.833A>T	ENSP00000358470.3:p.Tyr278Phe
ENST00000539893.5:c.548A>T	ENSP00000444724.1:p.Tyr183Phe
NM_001253849.1:c.548A>T	NP_001240778.1:p.Tyr183Phe
NM_001253850.1:c.485A>T	NP_001240779.1:p.Tyr162Phe
NM_024626.3:c.833A>T	NP_078902.2:p.Tyr278Phe
NR_045603.1:n.1028A>T
NR_045604.1:n.732A>T
XM_011542143.1:c.884A>T	XP_011540445.1:p.Tyr295Phe
XM_011542144.1:c.887A>T	XP_011540446.1:p.Tyr296Phe
XM_011542145.1:c.848A>T	XP_011540447.1:p.Tyr283Phe
XM_011542143.2:c.983A>T	XP_011540445.2:p.Tyr328Phe
XM_017002335.2:c.848A>T	XP_016857824.1:p.Tyr283Phe
NM_024626.4:c.833A>T MANE Select	NP_078902.2:p.Tyr278Phe
NR_045603.2:n.995A>T
NR_045604.2:n.699A>T
NM_001253849.2:c.548A>T	NP_001240778.1:p.Tyr183Phe
NM_001253850.2:c.485A>T	NP_001240779.1:p.Tyr162Phe