Canonical Allele Identifier: CA2664400078

Gene: VHL

Linked Data

• gnomAD v4: 3-10149771-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149776del , CM000665.2:g.10149776del	GRCh38
NC_000003.11:g.10191460del , CM000665.1:g.10191460del	GRCh37
NC_000003.10:g.10166460del	NCBI36
NG_008212.3:g.13142del , LRG_322:g.13142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*141-11del	ENSP00000512434.1:n.*141-11del
ENST00000696143.1:c.600-11del	ENSP00000512435.1:n.600-11del
ENST00000696153.1:c.575-11del	ENSP00000512444.1:n.575-11del
ENST00000256474.3:c.464-11del MANE Select	ENSP00000256474.3:n.464-11del
ENST00000256474.2:c.464-11del	ENSP00000256474.2:n.464-11del
ENST00000345392.2:c.341-11del	ENSP00000344757.2:n.341-11del
ENST00000477538.1:n.600-11del
NM_000551.3:c.464-11del , LRG_322t1:c.464-11del	NP_000542.1:n.464-11del
NM_198156.2:c.341-11del	NP_937799.1:n.341-11del
NM_001354723.1:c.*18-11del	NP_001341652.1:n.*18-11del
NM_000551.4:c.464-11del MANE Select	NP_000542.1:n.464-11del
NM_001354723.2:c.*18-11del	NP_001341652.1:n.*18-11del
NM_198156.3:c.341-11del	NP_937799.1:n.341-11del