Canonical Allele Identifier: CA913184902

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10142185_10142196del , CM000665.2:g.10142185_10142196del	GRCh38
NC_000003.11:g.10183869_10183880del , CM000665.1:g.10183869_10183880del	GRCh37
NC_000003.10:g.10158869_10158880del	NCBI36
NG_008212.3:g.5551_5562del , LRG_322:g.5551_5562del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.338_340+9del
ENST00000696143.1:c.338_340+9del
ENST00000696153.1:c.338_340+9del
ENST00000256474.3:c.338_340+9del
ENST00000256474.2:c.338_340+9del
ENST00000345392.2:c.338_340+9del
NM_000551.3:c.338_340+9del , LRG_322t1:c.338_340+9del
NM_198156.2:c.338_340+9del
XM_011534078.1:c.338_340+9del
NM_001354723.1:c.338_340+9del
NM_000551.4:c.338_340+9del
NM_001354723.2:c.338_340+9del
NM_198156.3:c.338_340+9del