Canonical Allele Identifier: CA1345063502
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10150308G= , CM000665.2:g.10150308G= GRCh38
NC_000003.11:g.10191992G= , CM000665.1:g.10191992G= GRCh37
NC_000003.10:g.10166992G= NCBI36
NG_008212.3:g.13674G= , LRG_322:g.13674G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*662G= ENSP00000512434.1:n.*662G=
ENST00000696143.1:c.1121G= ENSP00000512435.1:n.1121G=
ENST00000696153.1:c.*343G= ENSP00000512444.1:n.*343G=
ENST00000256474.3:c.*343G= MANE Select ENSP00000256474.3:n.*343G=
ENST00000256474.2:c.*343G= ENSP00000256474.2:n.*343G=
ENST00000345392.2:c.*343G= ENSP00000344757.2:n.*343G=
NM_000551.3:c.*343G= , LRG_322t1:c.*343G= NP_000542.1:n.*343G=
NM_198156.2:c.*343G= NP_937799.1:n.*343G=
NM_001354723.1:c.*539G= NP_001341652.1:n.*539G=
NM_000551.4:c.*343G= MANE Select NP_000542.1:n.*343G=
NM_001354723.2:c.*539G= NP_001341652.1:n.*539G=
NM_198156.3:c.*343G= NP_937799.1:n.*343G=