Canonical Allele Identifier: CA1345062357
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149824G= , CM000665.2:g.10149824G= GRCh38
NC_000003.11:g.10191508G= , CM000665.1:g.10191508G= GRCh37
NC_000003.10:g.10166508G= NCBI36
NG_008212.3:g.13190G= , LRG_322:g.13190G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*178G= ENSP00000512434.1:n.*178G=
ENST00000696143.1:c.637G= ENSP00000512435.1:n.637G=
ENST00000696153.1:c.612G= ENSP00000512444.1:p.Arg204=
ENST00000256474.3:c.501G= MANE Select ENSP00000256474.3:p.Arg167=
ENST00000256474.2:c.501G= ENSP00000256474.2:p.Arg167=
ENST00000345392.2:c.378G= ENSP00000344757.2:p.Arg126=
ENST00000477538.1:n.637G=
NM_000551.3:c.501G= , LRG_322t1:c.501G= NP_000542.1:p.Arg167=
NM_198156.2:c.378G= NP_937799.1:p.Arg126=
NM_001354723.1:c.*55G= NP_001341652.1:n.*55G=
NM_000551.4:c.501G= MANE Select NP_000542.1:p.Arg167=
NM_001354723.2:c.*55G= NP_001341652.1:n.*55G=
NM_198156.3:c.378G= NP_937799.1:p.Arg126=