Canonical Allele Identifier: CA1345060504
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10148270T= , CM000665.2:g.10148270T= GRCh38
NC_000003.11:g.10189954T= , CM000665.1:g.10189954T= GRCh37
NC_000003.10:g.10164954T= NCBI36
NG_008212.3:g.11636T= , LRG_322:g.11636T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.*141-1517T= ENSP00000512434.1:n.*141-1517T=
ENST00000696143.1:c.600-1517T= ENSP00000512435.1:n.600-1517T=
ENST00000696153.1:c.464-434T= ENSP00000512444.1:n.464-434T=
ENST00000256474.3:c.464-1517T= MANE Select ENSP00000256474.3:n.464-1517T=
ENST00000256474.2:c.464-1517T= ENSP00000256474.2:n.464-1517T=
ENST00000345392.2:c.341-1517T= ENSP00000344757.2:n.341-1517T=
ENST00000477538.1:n.600-1517T=
NM_000551.3:c.464-1517T= , LRG_322t1:c.464-1517T= NP_000542.1:n.464-1517T=
NM_198156.2:c.341-1517T= NP_937799.1:n.341-1517T=
NM_001354723.1:c.*18-1517T= NP_001341652.1:n.*18-1517T=
NM_000551.4:c.464-1517T= MANE Select NP_000542.1:n.464-1517T=
NM_001354723.2:c.*18-1517T= NP_001341652.1:n.*18-1517T=
NM_198156.3:c.341-1517T= NP_937799.1:n.341-1517T=