Canonical Allele Identifier: CA1345062775
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149901A= , CM000665.2:g.10149901A= GRCh38
NC_000003.11:g.10191585A= , CM000665.1:g.10191585A= GRCh37
NC_000003.10:g.10166585A= NCBI36
NG_008212.3:g.13267A= , LRG_322:g.13267A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*255A= ENSP00000512434.1:n.*255A=
ENST00000696143.1:c.714A= ENSP00000512435.1:n.714A=
ENST00000696153.1:c.689A= ENSP00000512444.1:p.Asn230=
ENST00000256474.3:c.578A= MANE Select ENSP00000256474.3:p.Asn193=
ENST00000256474.2:c.578A= ENSP00000256474.2:p.Asn193=
ENST00000345392.2:c.455A= ENSP00000344757.2:p.Asn152=
ENST00000477538.1:n.714A=
NM_000551.3:c.578A= , LRG_322t1:c.578A= NP_000542.1:p.Asn193=
NM_198156.2:c.455A= NP_937799.1:p.Asn152=
NM_001354723.1:c.*132A= NP_001341652.1:n.*132A=
NM_000551.4:c.578A= MANE Select NP_000542.1:p.Asn193=
NM_001354723.2:c.*132A= NP_001341652.1:n.*132A=
NM_198156.3:c.455A= NP_937799.1:p.Asn152=