Canonical Allele Identifier: CA2664402365

Gene: VHL

Linked Data

• gnomAD v4: 3-10151900-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10151906del , CM000665.2:g.10151906del	GRCh38
NC_000003.11:g.10193590del , CM000665.1:g.10193590del	GRCh37
NC_000003.10:g.10168590del	NCBI36
NG_008212.3:g.15272del , LRG_322:g.15272del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696143.1:c.2719del	ENSP00000512435.1:n.2719del
ENST00000696153.1:c.*1941del	ENSP00000512444.1:n.*1941del
ENST00000256474.3:c.*1941del MANE Select	ENSP00000256474.3:n.*1941del
ENST00000256474.2:c.*1941del	ENSP00000256474.2:n.*1941del
ENST00000345392.2:c.*1941del	ENSP00000344757.2:n.*1941del
NM_000551.3:c.*1941del , LRG_322t1:c.*1941del	NP_000542.1:n.*1941del
NM_198156.2:c.*1941del	NP_937799.1:n.*1941del
NM_001354723.1:c.*2137del	NP_001341652.1:n.*2137del
NM_000551.4:c.*1941del MANE Select	NP_000542.1:n.*1941del
NM_001354723.2:c.*2137del	NP_001341652.1:n.*2137del
NM_198156.3:c.*1941del	NP_937799.1:n.*1941del