Canonical Allele Identifier: CA1345065571
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152885G= , CM000665.2:g.10152885G= GRCh38
NC_000003.11:g.10194569G= , CM000665.1:g.10194569G= GRCh37
NC_000003.10:g.10169569G= NCBI36
NG_008212.3:g.16251G= , LRG_322:g.16251G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*2920G= ENSP00000512444.1:n.*2920G=
ENST00000256474.3:c.*2920G= MANE Select ENSP00000256474.3:n.*2920G=
NM_000551.3:c.*2920G= , LRG_322t1:c.*2920G= NP_000542.1:n.*2920G=
NM_198156.2:c.*2920G= NP_937799.1:n.*2920G=
NM_001354723.1:c.*3116G= NP_001341652.1:n.*3116G=
NM_000551.4:c.*2920G= MANE Select NP_000542.1:n.*2920G=
NM_001354723.2:c.*3116G= NP_001341652.1:n.*3116G=
NM_198156.3:c.*2920G= NP_937799.1:n.*2920G=