Canonical Allele Identifier: CA896159935

Gene: VHL

Linked Data

• dbSNP Id: rs1442820614
• MyVariant Identifiers: chr3:g.10184135_10184141del (hg19) ; chr3:g.10142451_10142457del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142451_10142457del , CM000665.2:g.10142451_10142457del	GRCh38
NC_000003.11:g.10184135_10184141del , CM000665.1:g.10184135_10184141del	GRCh37
NC_000003.10:g.10159135_10159141del	NCBI36
NG_008212.3:g.5817_5823del , LRG_322:g.5817_5823del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.340+264_340+270del	ENSP00000512434.1:n.340+264_340+270del
ENST00000696143.1:c.340+264_340+270del	ENSP00000512435.1:n.340+264_340+270del
ENST00000696153.1:c.340+264_340+270del	ENSP00000512444.1:n.340+264_340+270del
ENST00000256474.3:c.340+264_340+270del MANE Select	ENSP00000256474.3:n.340+264_340+270del
ENST00000256474.2:c.340+264_340+270del	ENSP00000256474.2:n.340+264_340+270del
ENST00000345392.2:c.340+264_340+270del	ENSP00000344757.2:n.340+264_340+270del
NM_000551.3:c.340+264_340+270del , LRG_322t1:c.340+264_340+270del	NP_000542.1:n.340+264_340+270del
NM_198156.2:c.340+264_340+270del	NP_937799.1:n.340+264_340+270del
XM_011534078.1:c.340+264_340+270del	XP_011532380.1:n.340+264_340+270del
NM_001354723.1:c.340+264_340+270del	NP_001341652.1:n.340+264_340+270del
NM_000551.4:c.340+264_340+270del MANE Select	NP_000542.1:n.340+264_340+270del
NM_001354723.2:c.340+264_340+270del	NP_001341652.1:n.340+264_340+270del
NM_198156.3:c.340+264_340+270del	NP_937799.1:n.340+264_340+270del