Canonical Allele Identifier: CA1345065020

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141903_10141904delinsGC , CM000665.2:g.10141903_10141904delinsGC	GRCh38
NC_000003.11:g.10183587_10183588delinsGC , CM000665.1:g.10183587_10183588delinsGC	GRCh37
NC_000003.10:g.10158587_10158588delinsGC	NCBI36
NG_008212.3:g.5269_5270delinsGC , LRG_322:g.5269_5270delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.56_57delinsGC	ENSP00000512434.1:p.Gly19=
ENST00000696143.1:c.56_57delinsGC	ENSP00000512435.1:p.Gly19=
ENST00000696153.1:c.56_57delinsGC	ENSP00000512444.1:p.Gly19=
ENST00000256474.3:c.56_57delinsGC MANE Select	ENSP00000256474.3:p.Gly19=
ENST00000256474.2:c.56_57delinsGC	ENSP00000256474.2:p.Gly19=
ENST00000345392.2:c.56_57delinsGC	ENSP00000344757.2:p.Gly19=
NM_000551.3:c.56_57delinsGC , LRG_322t1:c.56_57delinsGC	NP_000542.1:p.Gly19=
NM_198156.2:c.56_57delinsGC	NP_937799.1:p.Gly19=
XM_011534078.1:c.56_57delinsGC	XP_011532380.1:p.Gly19=
NM_001354723.1:c.56_57delinsGC	NP_001341652.1:p.Gly19=
NM_000551.4:c.56_57delinsGC MANE Select	NP_000542.1:p.Gly19=
NM_001354723.2:c.56_57delinsGC	NP_001341652.1:p.Gly19=
NM_198156.3:c.56_57delinsGC	NP_937799.1:p.Gly19=