Canonical Allele Identifier: CA1030291
Gene: VTCN1 HGNC NCBI

Linked Data

dbSNP Id: rs780253875

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.117147632G>T , CM000663.2:g.117147632G>T GRCh38
NC_000001.10:g.117690254G>T , CM000663.1:g.117690254G>T GRCh37
NC_000001.9:g.117491777G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369458.8:c.*26C>A MANE Select ENSP00000358470.3:n.*26C>A
ENST00000328189.7:c.*26C>A ENSP00000328168.3:n.*26C>A
ENST00000359008.8:c.*26C>A ENSP00000351899.4:n.*26C>A
ENST00000369458.7:c.*26C>A ENSP00000358470.3:n.*26C>A
ENST00000539893.5:c.*26C>A ENSP00000444724.1:n.*26C>A
NM_001253849.1:c.*26C>A NP_001240778.1:n.*26C>A
NM_001253850.1:c.*26C>A NP_001240779.1:n.*26C>A
NM_024626.3:c.*26C>A NP_078902.2:n.*26C>A
NR_045603.1:n.1070C>A
NR_045604.1:n.774C>A
XM_011542143.1:c.*26C>A XP_011540445.1:n.*26C>A
XM_011542144.1:c.*26C>A XP_011540446.1:n.*26C>A
XM_011542145.1:c.*26C>A XP_011540447.1:n.*26C>A
XM_011542143.2:c.*26C>A XP_011540445.2:n.*26C>A
XM_017002335.2:c.*26C>A XP_016857824.1:n.*26C>A
NM_024626.4:c.*26C>A MANE Select NP_078902.2:n.*26C>A
NR_045603.2:n.1037C>A
NR_045604.2:n.741C>A
NM_001253849.2:c.*26C>A NP_001240778.1:n.*26C>A
NM_001253850.2:c.*26C>A NP_001240779.1:n.*26C>A