Canonical Allele Identifier: CA2526632248
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811640_192811641insGTTT , CM000663.2:g.192811640_192811641insGTTT GRCh38
NC_000001.10:g.192780770_192780771insGTTT , CM000663.1:g.192780770_192780771insGTTT GRCh37
NC_000001.9:g.191047393_191047394insGTTT NCBI36
NG_012800.1:g.7602_7603insGTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*44_*45insGTTT MANE Select ENSP00000235382.5:n.*44_*45insGTTT
ENST00000235382.6:c.*44_*45insGTTT ENSP00000235382.5:n.*44_*45insGTTT
NM_002923.3:c.*44_*45insGTTT NP_002914.1:n.*44_*45insGTTT
NM_002923.4:c.*44_*45insGTTT MANE Select NP_002914.1:n.*44_*45insGTTT