Canonical Allele Identifier: CA523583527
Gene: RAVER2 HGNC NCBI

Linked Data

dbSNP Id: rs1326046288

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833095_64833096insGTC , CM000663.2:g.64833095_64833096insGTC GRCh38
NC_000001.10:g.65298778_65298779insGTC , CM000663.1:g.65298778_65298779insGTC GRCh37
NC_000001.9:g.65071366_65071367insGTC NCBI36
NG_023402.1:g.138409_138410insGAC
NG_023402.2:g.239651_239652insGAC

Transcript Alleles

HGVS Amino-acid change
ENST00000294428.8:c.*2110_*2111insGTC MANE Select ENSP00000294428.3:n.*2110_*2111insGTC
ENST00000294428.7:c.*2110_*2111insGTC ENSP00000294428.3:n.*2110_*2111insGTC
ENST00000371072.8:c.*2110_*2111insGTC ENSP00000360112.4:n.*2110_*2111insGTC
NM_018211.3:c.*2110_*2111insGTC NP_060681.2:n.*2110_*2111insGTC
XM_006710738.2:c.*2110_*2111insGTC XP_006710801.2:n.*2110_*2111insGTC
NM_001366165.1:c.*2110_*2111insGTC NP_001353094.1:n.*2110_*2111insGTC
XR_946693.3:n.4529_4530insGTC
NM_018211.4:c.*2110_*2111insGTC NP_060681.2:n.*2110_*2111insGTC
NM_001366165.2:c.*2110_*2111insGTC MANE Select NP_001353094.1:n.*2110_*2111insGTC