Canonical Allele Identifier: CA2577505249

Gene: VHL

Linked Data

• gnomAD v4: 3-10146656-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146661del , CM000665.2:g.10146661del	GRCh38
NC_000003.11:g.10188345del , CM000665.1:g.10188345del	GRCh37
NC_000003.10:g.10163345del	NCBI36
NG_008212.3:g.10027del , LRG_322:g.10027del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*140+25del	ENSP00000512434.1:n.*140+25del
ENST00000696143.1:c.600-3126del	ENSP00000512435.1:n.600-3126del
ENST00000696153.1:c.463+25del	ENSP00000512444.1:n.463+25del
ENST00000256474.3:c.463+25del MANE Select	ENSP00000256474.3:n.463+25del
ENST00000256474.2:c.463+25del	ENSP00000256474.2:n.463+25del
ENST00000345392.2:c.341-3126del	ENSP00000344757.2:n.341-3126del
ENST00000477538.1:n.599+25del
NM_000551.3:c.463+25del , LRG_322t1:c.463+25del	NP_000542.1:n.463+25del
NM_198156.2:c.341-3126del	NP_937799.1:n.341-3126del
NM_001354723.1:c.*18-3126del	NP_001341652.1:n.*18-3126del
NM_000551.4:c.463+25del MANE Select	NP_000542.1:n.463+25del
NM_001354723.2:c.*18-3126del	NP_001341652.1:n.*18-3126del
NM_198156.3:c.341-3126del	NP_937799.1:n.341-3126del