Canonical Allele Identifier: CA23896518
Gene: RAVER2 HGNC NCBI

Linked Data

dbSNP Id: rs1266504077
gnomAD v3: 1-64833087-A-AGTG
gnomAD v4: 1-64833087-A-AGTG
COSMIC: COSN15663174
MyVariant Identifiers: chr1:g.65298776_65298777insGTG (hg19) chr1:g.65298770_65298771insGTG (hg19) chr1:g.64833093_64833094insGTG (hg38) chr1:g.64833087_64833088insGTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833091_64833093dup , CM000663.2:g.64833091_64833093dup GRCh38
NC_000001.10:g.65298774_65298776dup , CM000663.1:g.65298774_65298776dup GRCh37
NC_000001.9:g.65071362_65071364dup NCBI36
NG_023402.1:g.138415_138417dup
NG_023402.2:g.239657_239659dup

Transcript Alleles

HGVS Amino-acid change
ENST00000294428.8:c.*2106_*2108dup MANE Select ENSP00000294428.3:n.*2106_*2108dup
ENST00000294428.7:c.*2106_*2108dup ENSP00000294428.3:n.*2106_*2108dup
ENST00000371072.8:c.*2106_*2108dup ENSP00000360112.4:n.*2106_*2108dup
NM_018211.3:c.*2106_*2108dup NP_060681.2:n.*2106_*2108dup
XM_006710738.2:c.*2106_*2108dup XP_006710801.2:n.*2106_*2108dup
NM_001366165.1:c.*2106_*2108dup NP_001353094.1:n.*2106_*2108dup
XR_946693.3:n.4525_4527dup
NM_018211.4:c.*2106_*2108dup NP_060681.2:n.*2106_*2108dup
NM_001366165.2:c.*2106_*2108dup MANE Select NP_001353094.1:n.*2106_*2108dup
Search 100 bp 5'
Search 100 bp 3'