Canonical Allele Identifier: CA432423359
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1365445365
MyVariant Identifiers: chr3:g.10191520G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149836G>A , CM000665.2:g.10149836G>A GRCh38
NC_000003.11:g.10191520G>A , CM000665.1:g.10191520G>A GRCh37
NC_000003.10:g.10166520G>A NCBI36
NG_008212.3:g.13202G>A , LRG_322:g.13202G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*190G>A ENSP00000512434.1:n.*190G>A
ENST00000696143.1:c.649G>A ENSP00000512435.1:n.649G>A
ENST00000696153.1:c.624G>A ENSP00000512444.1:p.Lys208=
ENST00000256474.3:c.513G>A MANE Select ENSP00000256474.3:p.Lys171=
ENST00000256474.2:c.513G>A ENSP00000256474.2:p.Lys171=
ENST00000345392.2:c.390G>A ENSP00000344757.2:p.Lys130=
ENST00000477538.1:n.649G>A
NM_000551.3:c.513G>A , LRG_322t1:c.513G>A NP_000542.1:p.Lys171=
NM_198156.2:c.390G>A NP_937799.1:p.Lys130=
NM_001354723.1:c.*67G>A NP_001341652.1:n.*67G>A
NM_000551.4:c.513G>A MANE Select NP_000542.1:p.Lys171=
NM_001354723.2:c.*67G>A NP_001341652.1:n.*67G>A
NM_198156.3:c.390G>A NP_937799.1:p.Lys130=