Canonical Allele Identifier: CA1345062348
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149823G= , CM000665.2:g.10149823G= GRCh38
NC_000003.11:g.10191507G= , CM000665.1:g.10191507G= GRCh37
NC_000003.10:g.10166507G= NCBI36
NG_008212.3:g.13189G= , LRG_322:g.13189G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*177G= ENSP00000512434.1:n.*177G=
ENST00000696143.1:c.636G= ENSP00000512435.1:n.636G=
ENST00000696153.1:c.611G= ENSP00000512444.1:p.Arg204=
ENST00000256474.3:c.500G= MANE Select ENSP00000256474.3:p.Arg167=
ENST00000256474.2:c.500G= ENSP00000256474.2:p.Arg167=
ENST00000345392.2:c.377G= ENSP00000344757.2:p.Arg126=
ENST00000477538.1:n.636G=
NM_000551.3:c.500G= , LRG_322t1:c.500G= NP_000542.1:p.Arg167=
NM_198156.2:c.377G= NP_937799.1:p.Arg126=
NM_001354723.1:c.*54G= NP_001341652.1:n.*54G=
NM_000551.4:c.500G= MANE Select NP_000542.1:p.Arg167=
NM_001354723.2:c.*54G= NP_001341652.1:n.*54G=
NM_198156.3:c.377G= NP_937799.1:p.Arg126=