Canonical Allele Identifier: CA2656451630
Gene: CACNG2 HGNC NCBI

Linked Data

gnomAD v4: 22-36564761-TGAA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564763_36564765del , CM000684.2:g.36564763_36564765del GRCh38
NC_000022.10:g.36960810_36960812del , CM000684.1:g.36960810_36960812del GRCh37
NC_000022.9:g.35290756_35290758del NCBI36
NG_031861.1:g.142880_142882del
NG_031861.2:g.143095_143097del

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.559_561del MANE Select ENSP00000300105.6:p.Phe187del
ENST00000300105.6:c.559_561del ENSP00000300105.6:p.Phe187del
NM_006078.3:c.559_561del NP_006069.1:p.Phe187del
NM_006078.4:c.559_561del NP_006069.1:p.Phe187del
XM_017028531.2:c.301_303del XP_016884020.1:p.Phe101del
NM_001379051.1:c.490_492del NP_001365980.1:p.Phe164del
NM_006078.5:c.559_561del MANE Select NP_006069.1:p.Phe187del
NR_166440.1:n.1925_1927del
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