Canonical Allele Identifier: CA2646050353
Gene: RAVER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833095_64833096insGTGTTGTT , CM000663.2:g.64833095_64833096insGTGTTGTT GRCh38
NC_000001.10:g.65298778_65298779insGTGTTGTT , CM000663.1:g.65298778_65298779insGTGTTGTT GRCh37
NC_000001.9:g.65071366_65071367insGTGTTGTT NCBI36
NG_023402.1:g.138413_138414insACACAACA
NG_023402.2:g.239655_239656insACACAACA

Transcript Alleles

HGVS Amino-acid change
ENST00000294428.8:c.*2110_*2111insGTGTTGTT MANE Select ENSP00000294428.3:n.*2110_*2111insGTGTTGT...
ENST00000294428.7:c.*2110_*2111insGTGTTGTT ENSP00000294428.3:n.*2110_*2111insGTGTTGT...
ENST00000371072.8:c.*2110_*2111insGTGTTGTT ENSP00000360112.4:n.*2110_*2111insGTGTTGT...
NM_018211.3:c.*2110_*2111insGTGTTGTT NP_060681.2:n.*2110_*2111insGTGTTGTT
XM_006710738.2:c.*2110_*2111insGTGTTGTT XP_006710801.2:n.*2110_*2111insGTGTTGTT
NM_001366165.1:c.*2110_*2111insGTGTTGTT NP_001353094.1:n.*2110_*2111insGTGTTGTT
XR_946693.3:n.4529_4530insGTGTTGTT
NM_018211.4:c.*2110_*2111insGTGTTGTT NP_060681.2:n.*2110_*2111insGTGTTGTT
NM_001366165.2:c.*2110_*2111insGTGTTGTT MANE Select NP_001353094.1:n.*2110_*2111insGTGTTGTT