Canonical Allele Identifier: CA70049183

Gene: VHL

Linked Data

• dbSNP Id: rs780199564
• MyVariant Identifiers: chr3:g.10187976G>A (hg19) ; chr3:g.10146292G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146292G>A , CM000665.2:g.10146292G>A	GRCh38
NC_000003.11:g.10187976G>A , CM000665.1:g.10187976G>A	GRCh37
NC_000003.10:g.10162976G>A	NCBI36
NG_008212.3:g.9658G>A , LRG_322:g.9658G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*18-222G>A	ENSP00000512434.1:n.*18-222G>A
ENST00000696143.1:c.599+3271G>A	ENSP00000512435.1:n.599+3271G>A
ENST00000696153.1:c.341-222G>A	ENSP00000512444.1:n.341-222G>A
ENST00000256474.3:c.341-222G>A MANE Select	ENSP00000256474.3:n.341-222G>A
ENST00000256474.2:c.341-222G>A	ENSP00000256474.2:n.341-222G>A
ENST00000345392.2:c.341-3495G>A	ENSP00000344757.2:n.341-3495G>A
ENST00000477538.1:n.477-222G>A
NM_000551.3:c.341-222G>A , LRG_322t1:c.341-222G>A	NP_000542.1:n.341-222G>A
NM_198156.2:c.341-3495G>A	NP_937799.1:n.341-3495G>A
XM_011534078.1:c.*18-222G>A	XP_011532380.1:n.*18-222G>A
NM_001354723.1:c.*17+3271G>A	NP_001341652.1:n.*17+3271G>A
NM_000551.4:c.341-222G>A MANE Select	NP_000542.1:n.341-222G>A
NM_001354723.2:c.*17+3271G>A	NP_001341652.1:n.*17+3271G>A
NM_198156.3:c.341-3495G>A	NP_937799.1:n.341-3495G>A