Canonical Allele Identifier: CA658795188
Gene: VHL HGNC NCBI

Linked Data

CIViC: CA658795188
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142020_10142021insC , CM000665.2:g.10142020_10142021insC GRCh38
NC_000003.11:g.10183704_10183705insC , CM000665.1:g.10183704_10183705insC GRCh37
NC_000003.10:g.10158704_10158705insC NCBI36
NG_008212.3:g.5386_5387insC , LRG_322:g.5386_5387insC

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.173_174insC ENSP00000512434.1:p.Pro59AlafsTer?
ENST00000696143.1:c.173_174insC ENSP00000512435.1:p.Pro59AlafsTer?
ENST00000696153.1:c.173_174insC ENSP00000512444.1:p.Pro59AlafsTer?
ENST00000256474.3:c.173_174insC MANE Select ENSP00000256474.3:p.Pro59AlafsTer?
ENST00000256474.2:c.173_174insC ENSP00000256474.2:p.Pro59AlafsTer?
ENST00000345392.2:c.173_174insC ENSP00000344757.2:p.Pro59AlafsTer?
NM_000551.3:c.173_174insC , LRG_322t1:c.173_174insC NP_000542.1:p.Pro59AlafsTer?
NM_198156.2:c.173_174insC NP_937799.1:p.Pro59AlafsTer?
XM_011534078.1:c.173_174insC XP_011532380.1:p.Pro59AlafsTer?
NM_001354723.1:c.173_174insC NP_001341652.1:p.Pro59AlafsTer?
NM_000551.4:c.173_174insC MANE Select NP_000542.1:p.Pro59AlafsTer?
NM_001354723.2:c.173_174insC NP_001341652.1:p.Pro59AlafsTer?
NM_198156.3:c.173_174insC NP_937799.1:p.Pro59AlafsTer?
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