Canonical Allele Identifier: CA645524624
Gene: VHL HGNC NCBI

Linked Data

COSMIC: COSM17729
MyVariant Identifiers: chr3:g.10183531_10183551del (hg19)
CIViC: CA645524624
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141847_10141867del , CM000665.2:g.10141847_10141867del GRCh38
NC_000003.11:g.10183531_10183551del , CM000665.1:g.10183531_10183551del GRCh37
NC_000003.10:g.10158531_10158551del NCBI36
NG_008212.3:g.5213_5233del , LRG_322:g.5213_5233del

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.-1_20del
ENST00000696153.1:c.-1_20del
ENST00000256474.3:c.-1_20del
ENST00000256474.2:c.-1_20del
ENST00000345392.2:c.-1_20del
NM_000551.3:c.-1_20del , LRG_322t1:c.-1_20del
NM_198156.2:c.-1_20del
XM_011534078.1:c.-1_20del
NM_001354723.1:c.-1_20del
NM_000551.4:c.-1_20del
NM_001354723.2:c.-1_20del
NM_198156.3:c.-1_20del
Search 100 bp 5'
Search 100 bp 3'