Canonical Allele Identifier: CA2664400367

Gene: VHL

Linked Data

• gnomAD v4: 3-10150407-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150407C>A , CM000665.2:g.10150407C>A	GRCh38
NC_000003.11:g.10192091C>A , CM000665.1:g.10192091C>A	GRCh37
NC_000003.10:g.10167091C>A	NCBI36
NG_008212.3:g.13773C>A , LRG_322:g.13773C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*761C>A	ENSP00000512434.1:n.*761C>A
ENST00000696143.1:c.1220C>A	ENSP00000512435.1:n.1220C>A
ENST00000696153.1:c.*442C>A	ENSP00000512444.1:n.*442C>A
ENST00000256474.3:c.*442C>A MANE Select	ENSP00000256474.3:n.*442C>A
ENST00000256474.2:c.*442C>A	ENSP00000256474.2:n.*442C>A
ENST00000345392.2:c.*442C>A	ENSP00000344757.2:n.*442C>A
NM_000551.3:c.*442C>A , LRG_322t1:c.*442C>A	NP_000542.1:n.*442C>A
NM_198156.2:c.*442C>A	NP_937799.1:n.*442C>A
NM_001354723.1:c.*638C>A	NP_001341652.1:n.*638C>A
NM_000551.4:c.*442C>A MANE Select	NP_000542.1:n.*442C>A
NM_001354723.2:c.*638C>A	NP_001341652.1:n.*638C>A
NM_198156.3:c.*442C>A	NP_937799.1:n.*442C>A