Canonical Allele Identifier: CA432421878

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10188279_10188280insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146596dup , CM000665.2:g.10146596dup	GRCh38
NC_000003.11:g.10188280dup , CM000665.1:g.10188280dup	GRCh37
NC_000003.10:g.10163280dup	NCBI36
NG_008212.3:g.9962dup , LRG_322:g.9962dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*100dup	ENSP00000512434.1:n.*100dup
ENST00000696143.1:c.600-3191dup	ENSP00000512435.1:n.600-3191dup
ENST00000696153.1:c.423dup	ENSP00000512444.1:p.Val142CysfsTer2
ENST00000256474.3:c.423dup MANE Select	ENSP00000256474.3:p.Val142CysfsTer2
ENST00000256474.2:c.423dup	ENSP00000256474.2:p.Val142CysfsTer2
ENST00000345392.2:c.341-3191dup	ENSP00000344757.2:n.341-3191dup
ENST00000477538.1:n.559dup
NM_000551.3:c.423dup , LRG_322t1:c.423dup	NP_000542.1:p.Val142CysfsTer2
NM_198156.2:c.341-3191dup	NP_937799.1:n.341-3191dup
XM_011534078.1:c.*100dup	XP_011532380.1:n.*100dup
NM_001354723.1:c.*18-3191dup	NP_001341652.1:n.*18-3191dup
NM_000551.4:c.423dup MANE Select	NP_000542.1:p.Val142CysfsTer2
NM_001354723.2:c.*18-3191dup	NP_001341652.1:n.*18-3191dup
NM_198156.3:c.341-3191dup	NP_937799.1:n.341-3191dup