Canonical Allele Identifier: CA1345065135
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141929G= , CM000665.2:g.10141929G= GRCh38
NC_000003.11:g.10183613G= , CM000665.1:g.10183613G= GRCh37
NC_000003.10:g.10158613G= NCBI36
NG_008212.3:g.5295G= , LRG_322:g.5295G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.82G= ENSP00000512434.1:p.Asp28=
ENST00000696143.1:c.82G= ENSP00000512435.1:p.Asp28=
ENST00000696153.1:c.82G= ENSP00000512444.1:p.Asp28=
ENST00000256474.3:c.82G= MANE Select ENSP00000256474.3:p.Asp28=
ENST00000256474.2:c.82G= ENSP00000256474.2:p.Asp28=
ENST00000345392.2:c.82G= ENSP00000344757.2:p.Asp28=
NM_000551.3:c.82G= , LRG_322t1:c.82G= NP_000542.1:p.Asp28=
NM_198156.2:c.82G= NP_937799.1:p.Asp28=
XM_011534078.1:c.82G= XP_011532380.1:p.Asp28=
NM_001354723.1:c.82G= NP_001341652.1:p.Asp28=
NM_000551.4:c.82G= MANE Select NP_000542.1:p.Asp28=
NM_001354723.2:c.82G= NP_001341652.1:p.Asp28=
NM_198156.3:c.82G= NP_937799.1:p.Asp28=