Canonical Allele Identifier: CA1215986918

Gene: RGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192812212_192812216delinsCAGCT , CM000663.2:g.192812212_192812216delinsCAGCT	GRCh38
NC_000001.10:g.192781342_192781346delinsCAGCT , CM000663.1:g.192781342_192781346delinsCAGCT	GRCh37
NC_000001.9:g.191047965_191047969delinsCAGCT	NCBI36
NG_012800.1:g.8174_8178delinsCAGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.7:c.*616_*620delinsCAGCT MANE Select	ENSP00000235382.5:n.*616_*620delinsCAGCT
ENST00000235382.6:c.*616_*620delinsCAGCT	ENSP00000235382.5:n.*616_*620delinsCAGCT
NM_002923.3:c.*616_*620delinsCAGCT	NP_002914.1:n.*616_*620delinsCAGCT
NM_002923.4:c.*616_*620delinsCAGCT MANE Select	NP_002914.1:n.*616_*620delinsCAGCT