Canonical Allele Identifier: CA1345062756
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149898C= , CM000665.2:g.10149898C= GRCh38
NC_000003.11:g.10191582C= , CM000665.1:g.10191582C= GRCh37
NC_000003.10:g.10166582C= NCBI36
NG_008212.3:g.13264C= , LRG_322:g.13264C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*252C= ENSP00000512434.1:n.*252C=
ENST00000696143.1:c.711C= ENSP00000512435.1:n.711C=
ENST00000696153.1:c.686C= ENSP00000512444.1:p.Pro229=
ENST00000256474.3:c.575C= MANE Select ENSP00000256474.3:p.Pro192=
ENST00000256474.2:c.575C= ENSP00000256474.2:p.Pro192=
ENST00000345392.2:c.452C= ENSP00000344757.2:p.Pro151=
ENST00000477538.1:n.711C=
NM_000551.3:c.575C= , LRG_322t1:c.575C= NP_000542.1:p.Pro192=
NM_198156.2:c.452C= NP_937799.1:p.Pro151=
NM_001354723.1:c.*129C= NP_001341652.1:n.*129C=
NM_000551.4:c.575C= MANE Select NP_000542.1:p.Pro192=
NM_001354723.2:c.*129C= NP_001341652.1:n.*129C=
NM_198156.3:c.452C= NP_937799.1:p.Pro151=