Canonical Allele Identifier: CA432536406

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10183729_10183730insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142045_10142046insT , CM000665.2:g.10142045_10142046insT	GRCh38
NC_000003.11:g.10183729_10183730insT , CM000665.1:g.10183729_10183730insT	GRCh37
NC_000003.10:g.10158729_10158730insT	NCBI36
NG_008212.3:g.5411_5412insT , LRG_322:g.5411_5412insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.198_199insT	ENSP00000512434.1:p.Asn67Ter
ENST00000696143.1:c.198_199insT	ENSP00000512435.1:p.Asn67Ter
ENST00000696153.1:c.198_199insT	ENSP00000512444.1:p.Asn67Ter
ENST00000256474.3:c.198_199insT MANE Select	ENSP00000256474.3:p.Asn67Ter
ENST00000256474.2:c.198_199insT	ENSP00000256474.2:p.Asn67Ter
ENST00000345392.2:c.198_199insT	ENSP00000344757.2:p.Asn67Ter
NM_000551.3:c.198_199insT , LRG_322t1:c.198_199insT	NP_000542.1:p.Asn67Ter
NM_198156.2:c.198_199insT	NP_937799.1:p.Asn67Ter
XM_011534078.1:c.198_199insT	XP_011532380.1:p.Asn67Ter
NM_001354723.1:c.198_199insT	NP_001341652.1:p.Asn67Ter
NM_000551.4:c.198_199insT MANE Select	NP_000542.1:p.Asn67Ter
NM_001354723.2:c.198_199insT	NP_001341652.1:p.Asn67Ter
NM_198156.3:c.198_199insT	NP_937799.1:p.Asn67Ter