Canonical Allele Identifier: CA1345064517
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141792_10141793delinsCG , CM000665.2:g.10141792_10141793delinsCG GRCh38
NC_000003.11:g.10183476_10183477delinsCG , CM000665.1:g.10183476_10183477delinsCG GRCh37
NC_000003.10:g.10158476_10158477delinsCG NCBI36
NG_008212.3:g.5158_5159delinsCG , LRG_322:g.5158_5159delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.-56_-55delinsCG ENSP00000512434.1:n.-56_-55delinsCG
ENST00000696153.1:c.-56_-55delinsCG ENSP00000512444.1:n.-56_-55delinsCG
ENST00000256474.3:c.-56_-55delinsCG MANE Select ENSP00000256474.3:n.-56_-55delinsCG
ENST00000256474.2:c.-56_-55delinsCG ENSP00000256474.2:n.-56_-55delinsCG
ENST00000345392.2:c.-56_-55delinsCG ENSP00000344757.2:n.-56_-55delinsCG
NM_000551.3:c.-56_-55delinsCG , LRG_322t1:c.-56_-55delinsCG NP_000542.1:n.-56_-55delinsCG
NM_198156.2:c.-56_-55delinsCG NP_937799.1:n.-56_-55delinsCG
XM_011534078.1:c.-56_-55delinsCG XP_011532380.1:n.-56_-55delinsCG
NM_001354723.1:c.-56_-55delinsCG NP_001341652.1:n.-56_-55delinsCG
NM_000551.4:c.-56_-55delinsCG MANE Select NP_000542.1:n.-56_-55delinsCG
NM_001354723.2:c.-56_-55delinsCG NP_001341652.1:n.-56_-55delinsCG
NM_198156.3:c.-56_-55delinsCG NP_937799.1:n.-56_-55delinsCG