Canonical Allele Identifier: CA29758376
Gene: VTCN1 HGNC NCBI

Linked Data

dbSNP Id: rs951992402

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.117147602A>G , CM000663.2:g.117147602A>G GRCh38
NC_000001.10:g.117690224A>G , CM000663.1:g.117690224A>G GRCh37
NC_000001.9:g.117491747A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369458.8:c.*45+11T>C MANE Select ENSP00000358470.3:n.*45+11T>C
ENST00000328189.7:c.*45+11T>C ENSP00000328168.3:n.*45+11T>C
ENST00000359008.8:c.*45+11T>C ENSP00000351899.4:n.*45+11T>C
ENST00000369458.7:c.*45+11T>C ENSP00000358470.3:n.*45+11T>C
ENST00000539893.5:c.*45+11T>C ENSP00000444724.1:n.*45+11T>C
NM_001253849.1:c.*45+11T>C NP_001240778.1:n.*45+11T>C
NM_001253850.1:c.*45+11T>C NP_001240779.1:n.*45+11T>C
NM_024626.3:c.*45+11T>C NP_078902.2:n.*45+11T>C
NR_045603.1:n.1089+11T>C
NR_045604.1:n.793+11T>C
XM_011542143.1:c.*45+11T>C XP_011540445.1:n.*45+11T>C
XM_011542144.1:c.*45+11T>C XP_011540446.1:n.*45+11T>C
XM_011542145.1:c.*45+11T>C XP_011540447.1:n.*45+11T>C
XM_011542143.2:c.*45+11T>C XP_011540445.2:n.*45+11T>C
XM_017002335.2:c.*45+11T>C XP_016857824.1:n.*45+11T>C
NM_024626.4:c.*45+11T>C MANE Select NP_078902.2:n.*45+11T>C
NR_045603.2:n.1056+11T>C
NR_045604.2:n.760+11T>C
NM_001253849.2:c.*45+11T>C NP_001240778.1:n.*45+11T>C
NM_001253850.2:c.*45+11T>C NP_001240779.1:n.*45+11T>C