Canonical Allele Identifier: CA2838255654
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141945dup , CM000665.2:g.10141945dup GRCh38
NC_000003.11:g.10183629dup , CM000665.1:g.10183629dup GRCh37
NC_000003.10:g.10158629dup NCBI36
NG_008212.3:g.5311dup , LRG_322:g.5311dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.98dup ENSP00000512434.1:p.Ala35ArgfsTer?
ENST00000696143.1:c.98dup ENSP00000512435.1:p.Ala35ArgfsTer?
ENST00000696153.1:c.98dup ENSP00000512444.1:p.Ala35ArgfsTer?
ENST00000256474.3:c.98dup MANE Select ENSP00000256474.3:p.Ala35ArgfsTer?
ENST00000256474.2:c.98dup ENSP00000256474.2:p.Ala35ArgfsTer?
ENST00000345392.2:c.98dup ENSP00000344757.2:p.Ala35ArgfsTer?
NM_000551.3:c.98dup , LRG_322t1:c.98dup NP_000542.1:p.Ala35ArgfsTer?
NM_198156.2:c.98dup NP_937799.1:p.Ala35ArgfsTer?
XM_011534078.1:c.98dup XP_011532380.1:p.Ala35ArgfsTer?
NM_001354723.1:c.98dup NP_001341652.1:p.Ala35ArgfsTer?
NM_000551.4:c.98dup MANE Select NP_000542.1:p.Ala35ArgfsTer?
NM_001354723.2:c.98dup NP_001341652.1:p.Ala35ArgfsTer?
NM_198156.3:c.98dup NP_937799.1:p.Ala35ArgfsTer?