Canonical Allele Identifier: CA1345064485

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141782_10141793delinsCTCCGCCCCGCG , CM000665.2:g.10141782_10141793delinsCTCCGCCCCGCG	GRCh38
NC_000003.11:g.10183466_10183477delinsCTCCGCCCCGCG , CM000665.1:g.10183466_10183477delinsCTCCGCCCCGCG	GRCh37
NC_000003.10:g.10158466_10158477delinsCTCCGCCCCGCG	NCBI36
NG_008212.3:g.5148_5159delinsCTCCGCCCCGCG , LRG_322:g.5148_5159delinsCTCCGCCCCGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696153.1:c.-66_-55delinsCTCCGCCCCGCG	ENSP00000512444.1:n.-66_-55delinsCTCCGCCCCGCG
ENST00000256474.3:c.-66_-55delinsCTCCGCCCCGCG MANE Select	ENSP00000256474.3:n.-66_-55delinsCTCCGCCCCGCG
ENST00000256474.2:c.-66_-55delinsCTCCGCCCCGCG	ENSP00000256474.2:n.-66_-55delinsCTCCGCCCCGCG
NM_000551.3:c.-66_-55delinsCTCCGCCCCGCG , LRG_322t1:c.-66_-55delinsCTCCGCCCCGCG	NP_000542.1:n.-66_-55delinsCTCCGCCCCGCG
NM_198156.2:c.-66_-55delinsCTCCGCCCCGCG	NP_937799.1:n.-66_-55delinsCTCCGCCCCGCG
XM_011534078.1:c.-66_-55delinsCTCCGCCCCGCG	XP_011532380.1:n.-66_-55delinsCTCCGCCCCGCG
NM_001354723.1:c.-66_-55delinsCTCCGCCCCGCG	NP_001341652.1:n.-66_-55delinsCTCCGCCCCGCG
NM_000551.4:c.-66_-55delinsCTCCGCCCCGCG MANE Select	NP_000542.1:n.-66_-55delinsCTCCGCCCCGCG
NM_001354723.2:c.-66_-55delinsCTCCGCCCCGCG	NP_001341652.1:n.-66_-55delinsCTCCGCCCCGCG
NM_198156.3:c.-66_-55delinsCTCCGCCCCGCG	NP_937799.1:n.-66_-55delinsCTCCGCCCCGCG