Canonical Allele Identifier: CA1345065173
Gene: VHL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152354G= , CM000665.2:g.10152354G= GRCh38
NC_000003.11:g.10194038G= , CM000665.1:g.10194038G= GRCh37
NC_000003.10:g.10169038G= NCBI36
NG_008212.3:g.15720G= , LRG_322:g.15720G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*2389G= ENSP00000512444.1:n.*2389G=
ENST00000256474.3:c.*2389G= MANE Select ENSP00000256474.3:n.*2389G=
NM_000551.3:c.*2389G= , LRG_322t1:c.*2389G= NP_000542.1:n.*2389G=
NM_198156.2:c.*2389G= NP_937799.1:n.*2389G=
NM_001354723.1:c.*2585G= NP_001341652.1:n.*2585G=
NM_000551.4:c.*2389G= MANE Select NP_000542.1:n.*2389G=
NM_001354723.2:c.*2585G= NP_001341652.1:n.*2585G=
NM_198156.3:c.*2389G= NP_937799.1:n.*2389G=
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