Canonical Allele Identifier: CA2832426654
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10146480_10149910del , CM000665.2:g.10146480_10149910del GRCh38
NC_000003.11:g.10188164_10191594del , CM000665.1:g.10188164_10191594del GRCh37
NC_000003.10:g.10163164_10166594del NCBI36
NG_008212.3:g.9846_13276del , LRG_322:g.9846_13276del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.*18-34_*264del
ENST00000696143.1:c.600-3307_723del
ENST00000696153.1:c.341-34_698del
ENST00000256474.3:c.341-34_587del
ENST00000256474.2:c.341-34_587del
ENST00000345392.2:c.341-3307_464del
ENST00000477538.1:n.477-34_723del
NM_000551.3:c.341-34_587del , LRG_322t1:c.341-34_587del
NM_198156.2:c.341-3307_464del
NM_001354723.1:c.*18-3307_*141del
NM_000551.4:c.341-34_587del
NM_001354723.2:c.*18-3307_*141del
NM_198156.3:c.341-3307_464del