Canonical Allele Identifier: CA2664400231
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10150258_10150259insAT , CM000665.2:g.10150258_10150259insAT GRCh38
NC_000003.11:g.10191942_10191943insAT , CM000665.1:g.10191942_10191943insAT GRCh37
NC_000003.10:g.10166942_10166943insAT NCBI36
NG_008212.3:g.13624_13625insAT , LRG_322:g.13624_13625insAT

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*612_*613insAT ENSP00000512434.1:n.*612_*613insAT
ENST00000696143.1:c.1071_1072insAT ENSP00000512435.1:n.1071_1072insAT
ENST00000696153.1:c.*293_*294insAT ENSP00000512444.1:n.*293_*294insAT
ENST00000256474.3:c.*293_*294insAT MANE Select ENSP00000256474.3:n.*293_*294insAT
ENST00000256474.2:c.*293_*294insAT ENSP00000256474.2:n.*293_*294insAT
ENST00000345392.2:c.*293_*294insAT ENSP00000344757.2:n.*293_*294insAT
NM_000551.3:c.*293_*294insAT , LRG_322t1:c.*293_*294insAT NP_000542.1:n.*293_*294insAT
NM_198156.2:c.*293_*294insAT NP_937799.1:n.*293_*294insAT
NM_001354723.1:c.*489_*490insAT NP_001341652.1:n.*489_*490insAT
NM_000551.4:c.*293_*294insAT MANE Select NP_000542.1:n.*293_*294insAT
NM_001354723.2:c.*489_*490insAT NP_001341652.1:n.*489_*490insAT
NM_198156.3:c.*293_*294insAT NP_937799.1:n.*293_*294insAT