Canonical Allele Identifier: CA523583543
Gene: RAVER2 HGNC NCBI

Linked Data

dbSNP Id: rs1263316388

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833148_64833149insGTTTTG , CM000663.2:g.64833148_64833149insGTTTTG GRCh38
NC_000001.10:g.65298831_65298832insGTTTTG , CM000663.1:g.65298831_65298832insGTTTTG GRCh37
NC_000001.9:g.65071419_65071420insGTTTTG NCBI36
NG_023402.1:g.138356_138357insCAAAAC
NG_023402.2:g.239598_239599insCAAAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000294428.8:c.*2163_*2164insGTTTTG MANE Select ENSP00000294428.3:n.*2163_*2164insGTTTTG
ENST00000294428.7:c.*2163_*2164insGTTTTG ENSP00000294428.3:n.*2163_*2164insGTTTTG
ENST00000371072.8:c.*2163_*2164insGTTTTG ENSP00000360112.4:n.*2163_*2164insGTTTTG
NM_018211.3:c.*2163_*2164insGTTTTG NP_060681.2:n.*2163_*2164insGTTTTG
XM_006710738.2:c.*2163_*2164insGTTTTG XP_006710801.2:n.*2163_*2164insGTTTTG
NM_001366165.1:c.*2163_*2164insGTTTTG NP_001353094.1:n.*2163_*2164insGTTTTG
XR_946693.3:n.4582_4583insGTTTTG
NM_018211.4:c.*2163_*2164insGTTTTG NP_060681.2:n.*2163_*2164insGTTTTG
NM_001366165.2:c.*2163_*2164insGTTTTG MANE Select NP_001353094.1:n.*2163_*2164insGTTTTG