Canonical Allele Identifier: CA1140698997
Gene: RAVER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833092_64833095delinsTGTT , CM000663.2:g.64833092_64833095delinsTGTT GRCh38
NC_000001.10:g.65298775_65298778delinsTGTT , CM000663.1:g.65298775_65298778delinsTGTT GRCh37
NC_000001.9:g.65071363_65071366delinsTGTT NCBI36
NG_023402.1:g.138410_138413delinsAACA
NG_023402.2:g.239652_239655delinsAACA

Transcript Alleles

HGVS Amino-acid change
ENST00000294428.8:c.*2107_*2110delinsTGTT MANE Select ENSP00000294428.3:n.*2107_*2110delinsTGTT...
ENST00000294428.7:c.*2107_*2110delinsTGTT ENSP00000294428.3:n.*2107_*2110delinsTGTT...
ENST00000371072.8:c.*2107_*2110delinsTGTT ENSP00000360112.4:n.*2107_*2110delinsTGTT...
NM_018211.3:c.*2107_*2110delinsTGTT NP_060681.2:n.*2107_*2110delinsTGTT
XM_006710738.2:c.*2107_*2110delinsTGTT XP_006710801.2:n.*2107_*2110delinsTGTT
NM_001366165.1:c.*2107_*2110delinsTGTT NP_001353094.1:n.*2107_*2110delinsTGTT
XR_946693.3:n.4526_4529delinsTGTT
NM_018211.4:c.*2107_*2110delinsTGTT NP_060681.2:n.*2107_*2110delinsTGTT
NM_001366165.2:c.*2107_*2110delinsTGTT MANE Select NP_001353094.1:n.*2107_*2110delinsTGTT