Canonical Allele Identifier: CA1345065379
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152603C= , CM000665.2:g.10152603C= GRCh38
NC_000003.11:g.10194287C= , CM000665.1:g.10194287C= GRCh37
NC_000003.10:g.10169287C= NCBI36
NG_008212.3:g.15969C= , LRG_322:g.15969C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*2638C= ENSP00000512444.1:n.*2638C=
ENST00000256474.3:c.*2638C= MANE Select ENSP00000256474.3:n.*2638C=
NM_000551.3:c.*2638C= , LRG_322t1:c.*2638C= NP_000542.1:n.*2638C=
NM_198156.2:c.*2638C= NP_937799.1:n.*2638C=
NM_001354723.1:c.*2834C= NP_001341652.1:n.*2834C=
NM_000551.4:c.*2638C= MANE Select NP_000542.1:n.*2638C=
NM_001354723.2:c.*2834C= NP_001341652.1:n.*2834C=
NM_198156.3:c.*2638C= NP_937799.1:n.*2638C=