Canonical Allele Identifier: CA915940707
Gene: VHL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142148_10142149delinsGG , CM000665.2:g.10142148_10142149delinsGG GRCh38
NC_000003.11:g.10183832_10183833delinsGG , CM000665.1:g.10183832_10183833delinsGG GRCh37
NC_000003.10:g.10158832_10158833delinsGG NCBI36
NG_008212.3:g.5514_5515delinsGG , LRG_322:g.5514_5515delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.301_302delinsGG ENSP00000512434.1:p.Leu101Gly
ENST00000696143.1:c.301_302delinsGG ENSP00000512435.1:p.Leu101Gly
ENST00000696153.1:c.301_302delinsGG ENSP00000512444.1:p.Leu101Gly
ENST00000256474.3:c.301_302delinsGG MANE Select ENSP00000256474.3:p.Leu101Gly
ENST00000256474.2:c.301_302delinsGG ENSP00000256474.2:p.Leu101Gly
ENST00000345392.2:c.301_302delinsGG ENSP00000344757.2:p.Leu101Gly
NM_000551.3:c.301_302delinsGG , LRG_322t1:c.301_302delinsGG NP_000542.1:p.Leu101Gly
NM_198156.2:c.301_302delinsGG NP_937799.1:p.Leu101Gly
XM_011534078.1:c.301_302delinsGG XP_011532380.1:p.Leu101Gly
NM_001354723.1:c.301_302delinsGG NP_001341652.1:p.Leu101Gly
NM_000551.4:c.301_302delinsGG MANE Select NP_000542.1:p.Leu101Gly
NM_001354723.2:c.301_302delinsGG NP_001341652.1:p.Leu101Gly
NM_198156.3:c.301_302delinsGG NP_937799.1:p.Leu101Gly