Canonical Allele Identifier: CA1345063498
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10150302A>C , CM000665.2:g.10150302A>C GRCh38
NC_000003.11:g.10191986A>C , CM000665.1:g.10191986A>C GRCh37
NC_000003.10:g.10166986A>C NCBI36
NG_008212.3:g.13668A>C , LRG_322:g.13668A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256474.3:c.*337A>C MANE Select ENSP00000256474.3:p.=
ENST00000256474.2:c.*337A>C ENSP00000256474.2:p.=
ENST00000345392.2:c.*337A>C ENSP00000344757.2:p.=
NM_000551.3:c.*337A>C , LRG_322t1:c.*337A>C NP_000542.1:p.=
NM_198156.2:c.*337A>C NP_937799.1:p.=
NM_001354723.1:c.*533A>C NP_001341652.1:p.=
NM_000551.4:c.*337A>C MANE Select NP_000542.1:p.=
NM_001354723.2:c.*533A>C NP_001341652.1:p.=
NM_198156.3:c.*337A>C NP_937799.1:p.=