Canonical Allele Identifier: CA1345065228
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152452G= , CM000665.2:g.10152452G= GRCh38
NC_000003.11:g.10194136G= , CM000665.1:g.10194136G= GRCh37
NC_000003.10:g.10169136G= NCBI36
NG_008212.3:g.15818G= , LRG_322:g.15818G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696153.1:c.*2487G= ENSP00000512444.1:n.*2487G=
ENST00000256474.3:c.*2487G= MANE Select ENSP00000256474.3:n.*2487G=
NM_000551.3:c.*2487G= , LRG_322t1:c.*2487G= NP_000542.1:n.*2487G=
NM_198156.2:c.*2487G= NP_937799.1:n.*2487G=
NM_001354723.1:c.*2683G= NP_001341652.1:n.*2683G=
NM_000551.4:c.*2487G= MANE Select NP_000542.1:n.*2487G=
NM_001354723.2:c.*2683G= NP_001341652.1:n.*2683G=
NM_198156.3:c.*2487G= NP_937799.1:n.*2487G=