Canonical Allele Identifier: CA1345065782
Gene: VHL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10153200C= , CM000665.2:g.10153200C= GRCh38
NC_000003.11:g.10194884C= , CM000665.1:g.10194884C= GRCh37
NC_000003.10:g.10169884C= NCBI36
NG_008212.3:g.16566C= , LRG_322:g.16566C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*3235C= ENSP00000512444.1:n.*3235C=
ENST00000256474.3:c.*3235C= MANE Select ENSP00000256474.3:n.*3235C=
NM_000551.3:c.*3235C= , LRG_322t1:c.*3235C= NP_000542.1:n.*3235C=
NM_198156.2:c.*3235C= NP_937799.1:n.*3235C=
NM_001354723.1:c.*3431C= NP_001341652.1:n.*3431C=
NM_000551.4:c.*3235C= MANE Select NP_000542.1:n.*3235C=
NM_001354723.2:c.*3431C= NP_001341652.1:n.*3431C=
NM_198156.3:c.*3235C= NP_937799.1:n.*3235C=
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