Canonical Allele Identifier: CA2664402054
Gene: VHL HGNC NCBI

Linked Data

gnomAD v4: 3-10142924-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142924G>T , CM000665.2:g.10142924G>T GRCh38
NC_000003.11:g.10184608G>T , CM000665.1:g.10184608G>T GRCh37
NC_000003.10:g.10159608G>T NCBI36
NG_008212.3:g.6290G>T , LRG_322:g.6290G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.502G>T ENSP00000512434.1:p.Ala168Ser
ENST00000696143.1:c.502G>T ENSP00000512435.1:p.Ala168Ser
ENST00000696153.1:c.340+737G>T ENSP00000512444.1:n.340+737G>T
ENST00000256474.3:c.340+737G>T MANE Select ENSP00000256474.3:n.340+737G>T
ENST00000256474.2:c.340+737G>T ENSP00000256474.2:n.340+737G>T
ENST00000345392.2:c.340+737G>T ENSP00000344757.2:n.340+737G>T
ENST00000477538.1:n.379G>T
NM_000551.3:c.340+737G>T , LRG_322t1:c.340+737G>T NP_000542.1:n.340+737G>T
NM_198156.2:c.340+737G>T NP_937799.1:n.340+737G>T
XM_011534078.1:c.502G>T XP_011532380.1:p.Ala168Ser
NM_001354723.1:c.502G>T NP_001341652.1:p.Ala168Ser
NM_000551.4:c.340+737G>T MANE Select NP_000542.1:n.340+737G>T
NM_001354723.2:c.502G>T NP_001341652.1:p.Ala168Ser
NM_198156.3:c.340+737G>T NP_937799.1:n.340+737G>T