Canonical Allele Identifier: CA737900666
Gene: RAVER2 HGNC NCBI

Linked Data

dbSNP Id: rs1553157366

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833098_64833099insGTGT , CM000663.2:g.64833098_64833099insGTGT GRCh38
NC_000001.10:g.65298781_65298782insGTGT , CM000663.1:g.65298781_65298782insGTGT GRCh37
NC_000001.9:g.65071369_65071370insGTGT NCBI36
NG_023402.1:g.138409_138410insCACA
NG_023402.2:g.239651_239652insCACA

Transcript Alleles

HGVS Amino-acid change
ENST00000294428.8:c.*2113_*2114insGTGT MANE Select ENSP00000294428.3:n.*2113_*2114insGTGT
ENST00000294428.7:c.*2113_*2114insGTGT ENSP00000294428.3:n.*2113_*2114insGTGT
ENST00000371072.8:c.*2113_*2114insGTGT ENSP00000360112.4:n.*2113_*2114insGTGT
NM_018211.3:c.*2113_*2114insGTGT NP_060681.2:n.*2113_*2114insGTGT
XM_006710738.2:c.*2113_*2114insGTGT XP_006710801.2:n.*2113_*2114insGTGT
NM_001366165.1:c.*2113_*2114insGTGT NP_001353094.1:n.*2113_*2114insGTGT
XR_946693.3:n.4532_4533insGTGT
NM_018211.4:c.*2113_*2114insGTGT NP_060681.2:n.*2113_*2114insGTGT
NM_001366165.2:c.*2113_*2114insGTGT MANE Select NP_001353094.1:n.*2113_*2114insGTGT