Canonical Allele Identifier: CA1345065325
Gene: VHL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152532G= , CM000665.2:g.10152532G= GRCh38
NC_000003.11:g.10194216G= , CM000665.1:g.10194216G= GRCh37
NC_000003.10:g.10169216G= NCBI36
NG_008212.3:g.15898G= , LRG_322:g.15898G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*2567G= ENSP00000512444.1:n.*2567G=
ENST00000256474.3:c.*2567G= MANE Select ENSP00000256474.3:n.*2567G=
NM_000551.3:c.*2567G= , LRG_322t1:c.*2567G= NP_000542.1:n.*2567G=
NM_198156.2:c.*2567G= NP_937799.1:n.*2567G=
NM_001354723.1:c.*2763G= NP_001341652.1:n.*2763G=
NM_000551.4:c.*2567G= MANE Select NP_000542.1:n.*2567G=
NM_001354723.2:c.*2763G= NP_001341652.1:n.*2763G=
NM_198156.3:c.*2567G= NP_937799.1:n.*2567G=
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