Canonical Allele Identifier: CA432536396
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM253340 COSM423175
MyVariant Identifiers: chr3:g.10183727del (hg19) chr3:g.10183726del (hg19)
CIViC: CA432536396
PCER: P-CER:CA432536396/193300
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142043del , CM000665.2:g.10142043del GRCh38
NC_000003.11:g.10183727del , CM000665.1:g.10183727del GRCh37
NC_000003.10:g.10158727del NCBI36
NG_008212.3:g.5409del , LRG_322:g.5409del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.196del ENSP00000512434.1:p.Val66Ter
ENST00000696143.1:c.196del ENSP00000512435.1:p.Val66Ter
ENST00000696153.1:c.196del ENSP00000512444.1:p.Val66Ter
ENST00000256474.3:c.196del MANE Select ENSP00000256474.3:p.Val66Ter
ENST00000256474.2:c.196del ENSP00000256474.2:p.Val66Ter
ENST00000345392.2:c.196del ENSP00000344757.2:p.Val66Ter
NM_000551.3:c.196del , LRG_322t1:c.196del NP_000542.1:p.Val66Ter
NM_198156.2:c.196del NP_937799.1:p.Val66Ter
XM_011534078.1:c.196del XP_011532380.1:p.Val66Ter
NM_001354723.1:c.196del NP_001341652.1:p.Val66Ter
NM_000551.4:c.196del MANE Select NP_000542.1:p.Val66Ter
NM_001354723.2:c.196del NP_001341652.1:p.Val66Ter
NM_198156.3:c.196del NP_937799.1:p.Val66Ter
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