Canonical Allele Identifier: CA2646050357
Gene: RAVER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833100_64833101insTTTT , CM000663.2:g.64833100_64833101insTTTT GRCh38
NC_000001.10:g.65298783_65298784insTTTT , CM000663.1:g.65298783_65298784insTTTT GRCh37
NC_000001.9:g.65071371_65071372insTTTT NCBI36
NG_023402.1:g.138407_138408insAAAA
NG_023402.2:g.239649_239650insAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000294428.8:c.*2115_*2116insTTTT MANE Select ENSP00000294428.3:n.*2115_*2116insTTTT
ENST00000294428.7:c.*2115_*2116insTTTT ENSP00000294428.3:n.*2115_*2116insTTTT
ENST00000371072.8:c.*2115_*2116insTTTT ENSP00000360112.4:n.*2115_*2116insTTTT
NM_018211.3:c.*2115_*2116insTTTT NP_060681.2:n.*2115_*2116insTTTT
XM_006710738.2:c.*2115_*2116insTTTT XP_006710801.2:n.*2115_*2116insTTTT
NM_001366165.1:c.*2115_*2116insTTTT NP_001353094.1:n.*2115_*2116insTTTT
XR_946693.3:n.4534_4535insTTTT
NM_018211.4:c.*2115_*2116insTTTT NP_060681.2:n.*2115_*2116insTTTT
NM_001366165.2:c.*2115_*2116insTTTT MANE Select NP_001353094.1:n.*2115_*2116insTTTT