Canonical Allele Identifier: CA1002570157
Gene: RAVER2 HGNC NCBI

Linked Data

dbSNP Id: rs1654220711

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833104_64833105insATTT , CM000663.2:g.64833104_64833105insATTT GRCh38
NC_000001.10:g.65298787_65298788insATTT , CM000663.1:g.65298787_65298788insATTT GRCh37
NC_000001.9:g.65071375_65071376insATTT NCBI36
NG_023402.1:g.138403_138404insTAAA
NG_023402.2:g.239645_239646insTAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000294428.8:c.*2119_*2120insATTT MANE Select ENSP00000294428.3:n.*2119_*2120insATTT
ENST00000294428.7:c.*2119_*2120insATTT ENSP00000294428.3:n.*2119_*2120insATTT
ENST00000371072.8:c.*2119_*2120insATTT ENSP00000360112.4:n.*2119_*2120insATTT
NM_018211.3:c.*2119_*2120insATTT NP_060681.2:n.*2119_*2120insATTT
XM_006710738.2:c.*2119_*2120insATTT XP_006710801.2:n.*2119_*2120insATTT
NM_001366165.1:c.*2119_*2120insATTT NP_001353094.1:n.*2119_*2120insATTT
XR_946693.3:n.4538_4539insATTT
NM_018211.4:c.*2119_*2120insATTT NP_060681.2:n.*2119_*2120insATTT
NM_001366165.2:c.*2119_*2120insATTT MANE Select NP_001353094.1:n.*2119_*2120insATTT