Canonical Allele Identifier: PA108921
Gene: VHL HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_000542.1:p.Phe76Leu
NM_000551.4:c.[224_225insA;226T=;228del]

NM_000551.4:c.[224_225insA;227del]

NM_000551.4:c.[224_225insA;227T>A;228del]...

NM_000551.4:c.[224_225insA;227T>C;228del]...

NM_000551.4:c.[224_225insA;227T>G;228del]...

NM_000551.4:c.[224_225insA;227T=;228del]

NM_000551.4:c.[224_225insA;228del]

NM_000551.4:c.[224dup;226T=;228del]

NM_000551.4:c.[224dup;227del]

NM_000551.4:c.[224dup;227T>A;228del]

NM_000551.4:c.[224dup;227T>C;228del]

NM_000551.4:c.[224dup;227T>G;228del]

NM_000551.4:c.[224dup;227T=;228del]

NM_000551.4:c.[224dup;228del]

NM_000551.4:c.[225dup;227del]

NM_000551.4:c.[225dup;227T>A;228del]

NM_000551.4:c.[225dup;227T>C;228del]

NM_000551.4:c.[225dup;227T>G;228del]

NM_000551.4:c.[225dup;227T=;228del]

NM_000551.4:c.[225dup;228del]

NM_000551.4:c.226T>C

NM_000551.4:c.228C>A

NM_000551.4:c.228C>G