Canonical Allele Identifier: CA2646050364
Gene: RAVER2 HGNC NCBI

Linked Data

gnomAD v4: 1-64833109-G-GTTTGT
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833110_64833111insTTGTT , CM000663.2:g.64833110_64833111insTTGTT GRCh38
NC_000001.10:g.65298793_65298794insTTGTT , CM000663.1:g.65298793_65298794insTTGTT GRCh37
NC_000001.9:g.65071381_65071382insTTGTT NCBI36
NG_023402.1:g.138395_138396insACAAA
NG_023402.2:g.239637_239638insACAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000294428.8:c.*2125_*2126insTTGTT MANE Select ENSP00000294428.3:n.*2125_*2126insTTGTT
ENST00000294428.7:c.*2125_*2126insTTGTT ENSP00000294428.3:n.*2125_*2126insTTGTT
ENST00000371072.8:c.*2125_*2126insTTGTT ENSP00000360112.4:n.*2125_*2126insTTGTT
NM_018211.3:c.*2125_*2126insTTGTT NP_060681.2:n.*2125_*2126insTTGTT
XM_006710738.2:c.*2125_*2126insTTGTT XP_006710801.2:n.*2125_*2126insTTGTT
NM_001366165.1:c.*2125_*2126insTTGTT NP_001353094.1:n.*2125_*2126insTTGTT
XR_946693.3:n.4544_4545insTTGTT
NM_018211.4:c.*2125_*2126insTTGTT NP_060681.2:n.*2125_*2126insTTGTT
NM_001366165.2:c.*2125_*2126insTTGTT MANE Select NP_001353094.1:n.*2125_*2126insTTGTT
Search 100 bp 5'
Search 100 bp 3'