Canonical Allele Identifier: CA647445648

Gene: VHL

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142571_10142572insA , CM000665.2:g.10142571_10142572insA	GRCh38
NC_000003.11:g.10184255_10184256insA , CM000665.1:g.10184255_10184256insA	GRCh37
NC_000003.10:g.10159255_10159256insA	NCBI36
NG_008212.3:g.5937_5938insA , LRG_322:g.5937_5938insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.341-192_341-191insA	ENSP00000512434.1:n.341-192_341-191insA
ENST00000696143.1:c.341-192_341-191insA	ENSP00000512435.1:n.341-192_341-191insA
ENST00000696153.1:c.340+384_340+385insA	ENSP00000512444.1:n.340+384_340+385insA
ENST00000256474.3:c.340+384_340+385insA MANE Select	ENSP00000256474.3:n.340+384_340+385insA
ENST00000256474.2:c.340+384_340+385insA	ENSP00000256474.2:n.340+384_340+385insA
ENST00000345392.2:c.340+384_340+385insA	ENSP00000344757.2:n.340+384_340+385insA
ENST00000477538.1:n.26_27insA
NM_000551.3:c.340+384_340+385insA , LRG_322t1:c.340+384_340+385insA	NP_000542.1:n.340+384_340+385insA
NM_198156.2:c.340+384_340+385insA	NP_937799.1:n.340+384_340+385insA
XM_011534078.1:c.341-192_341-191insA	XP_011532380.1:n.341-192_341-191insA
NM_001354723.1:c.341-192_341-191insA	NP_001341652.1:n.341-192_341-191insA
NM_000551.4:c.340+384_340+385insA MANE Select	NP_000542.1:n.340+384_340+385insA
NM_001354723.2:c.341-192_341-191insA	NP_001341652.1:n.341-192_341-191insA
NM_198156.3:c.340+384_340+385insA	NP_937799.1:n.340+384_340+385insA