Canonical Allele Identifier: CA2586965665

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142160_10142161dup , CM000665.2:g.10142160_10142161dup	GRCh38
NC_000003.11:g.10183844_10183845dup , CM000665.1:g.10183844_10183845dup	GRCh37
NC_000003.10:g.10158844_10158845dup	NCBI36
NG_008212.3:g.5526_5527dup , LRG_322:g.5526_5527dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.313_314dup	ENSP00000512434.1:p.Gly106ArgfsTer12
ENST00000696143.1:c.313_314dup	ENSP00000512435.1:p.Gly106ArgfsTer12
ENST00000696153.1:c.313_314dup	ENSP00000512444.1:p.Gly106ArgfsTer?
ENST00000256474.3:c.313_314dup MANE Select	ENSP00000256474.3:p.Gly106ArgfsTer?
ENST00000256474.2:c.313_314dup	ENSP00000256474.2:p.Gly106ArgfsTer?
ENST00000345392.2:c.313_314dup	ENSP00000344757.2:p.Gly106ArgfsTer13
NM_000551.3:c.313_314dup , LRG_322t1:c.313_314dup	NP_000542.1:p.Gly106ArgfsTer?
NM_198156.2:c.313_314dup	NP_937799.1:p.Gly106ArgfsTer13
XM_011534078.1:c.313_314dup	XP_011532380.1:p.Gly106ArgfsTer12
NM_001354723.1:c.313_314dup	NP_001341652.1:p.Gly106ArgfsTer12
NM_000551.4:c.313_314dup MANE Select	NP_000542.1:p.Gly106ArgfsTer?
NM_001354723.2:c.313_314dup	NP_001341652.1:p.Gly106ArgfsTer12
NM_198156.3:c.313_314dup	NP_937799.1:p.Gly106ArgfsTer13