Canonical Allele Identifier: CA2702124129

Gene: VHL

Linked Data

• dbSNP Id: rs2125124329

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141835del , CM000665.2:g.10141835del	GRCh38
NC_000003.11:g.10183519del , CM000665.1:g.10183519del	GRCh37
NC_000003.10:g.10158519del	NCBI36
NG_008212.3:g.5201del , LRG_322:g.5201del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.-13del	ENSP00000512434.1:n.-13del
ENST00000696153.1:c.-13del	ENSP00000512444.1:n.-13del
ENST00000256474.3:c.-13del MANE Select	ENSP00000256474.3:n.-13del
ENST00000256474.2:c.-13del	ENSP00000256474.2:n.-13del
ENST00000345392.2:c.-13del	ENSP00000344757.2:n.-13del
NM_000551.3:c.-13del , LRG_322t1:c.-13del	NP_000542.1:n.-13del
NM_198156.2:c.-13del	NP_937799.1:n.-13del
XM_011534078.1:c.-13del	XP_011532380.1:n.-13del
NM_001354723.1:c.-13del	NP_001341652.1:n.-13del
NM_000551.4:c.-13del MANE Select	NP_000542.1:n.-13del
NM_001354723.2:c.-13del	NP_001341652.1:n.-13del
NM_198156.3:c.-13del	NP_937799.1:n.-13del