Canonical Allele Identifier: CA1345062409
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149835A= , CM000665.2:g.10149835A= GRCh38
NC_000003.11:g.10191519A= , CM000665.1:g.10191519A= GRCh37
NC_000003.10:g.10166519A= NCBI36
NG_008212.3:g.13201A= , LRG_322:g.13201A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*189A= ENSP00000512434.1:n.*189A=
ENST00000696143.1:c.648A= ENSP00000512435.1:n.648A=
ENST00000696153.1:c.623A= ENSP00000512444.1:p.Lys208=
ENST00000256474.3:c.512A= MANE Select ENSP00000256474.3:p.Lys171=
ENST00000256474.2:c.512A= ENSP00000256474.2:p.Lys171=
ENST00000345392.2:c.389A= ENSP00000344757.2:p.Lys130=
ENST00000477538.1:n.648A=
NM_000551.3:c.512A= , LRG_322t1:c.512A= NP_000542.1:p.Lys171=
NM_198156.2:c.389A= NP_937799.1:p.Lys130=
NM_001354723.1:c.*66A= NP_001341652.1:n.*66A=
NM_000551.4:c.512A= MANE Select NP_000542.1:p.Lys171=
NM_001354723.2:c.*66A= NP_001341652.1:n.*66A=
NM_198156.3:c.389A= NP_937799.1:p.Lys130=