Canonical Allele Identifier: CA1345060822
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10148515C= , CM000665.2:g.10148515C= GRCh38
NC_000003.11:g.10190199C= , CM000665.1:g.10190199C= GRCh37
NC_000003.10:g.10165199C= NCBI36
NG_008212.3:g.11881C= , LRG_322:g.11881C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*141-1272C= ENSP00000512434.1:n.*141-1272C=
ENST00000696143.1:c.600-1272C= ENSP00000512435.1:n.600-1272C=
ENST00000696153.1:c.464-189C= ENSP00000512444.1:n.464-189C=
ENST00000256474.3:c.464-1272C= MANE Select ENSP00000256474.3:n.464-1272C=
ENST00000256474.2:c.464-1272C= ENSP00000256474.2:n.464-1272C=
ENST00000345392.2:c.341-1272C= ENSP00000344757.2:n.341-1272C=
ENST00000477538.1:n.600-1272C=
NM_000551.3:c.464-1272C= , LRG_322t1:c.464-1272C= NP_000542.1:n.464-1272C=
NM_198156.2:c.341-1272C= NP_937799.1:n.341-1272C=
NM_001354723.1:c.*18-1272C= NP_001341652.1:n.*18-1272C=
NM_000551.4:c.464-1272C= MANE Select NP_000542.1:n.464-1272C=
NM_001354723.2:c.*18-1272C= NP_001341652.1:n.*18-1272C=
NM_198156.3:c.341-1272C= NP_937799.1:n.341-1272C=