Canonical Allele Identifier: CA1345063440
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10150249A= , CM000665.2:g.10150249A= GRCh38
NC_000003.11:g.10191933A= , CM000665.1:g.10191933A= GRCh37
NC_000003.10:g.10166933A= NCBI36
NG_008212.3:g.13615A= , LRG_322:g.13615A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.*603A= ENSP00000512434.1:n.*603A=
ENST00000696143.1:c.1062A= ENSP00000512435.1:n.1062A=
ENST00000696153.1:c.*284A= ENSP00000512444.1:n.*284A=
ENST00000256474.3:c.*284A= MANE Select ENSP00000256474.3:n.*284A=
ENST00000256474.2:c.*284A= ENSP00000256474.2:n.*284A=
ENST00000345392.2:c.*284A= ENSP00000344757.2:n.*284A=
NM_000551.3:c.*284A= , LRG_322t1:c.*284A= NP_000542.1:n.*284A=
NM_198156.2:c.*284A= NP_937799.1:n.*284A=
NM_001354723.1:c.*480A= NP_001341652.1:n.*480A=
NM_000551.4:c.*284A= MANE Select NP_000542.1:n.*284A=
NM_001354723.2:c.*480A= NP_001341652.1:n.*480A=
NM_198156.3:c.*284A= NP_937799.1:n.*284A=