Canonical Allele Identifier: CA381531844
Community Standard Title: NM_001619.5(GRK2):c.555+1G>A
Gene: GRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67280784G>A , CM000673.2:g.67280784G>A GRCh38
NC_000011.9:g.67048255G>A , CM000673.1:g.67048255G>A GRCh37
NC_000011.8:g.66804831G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001619.5:c.555+1G>A MANE Select NP_001610.2:n.555+1G>A
ENST00000308595.10:c.555+1G>A MANE Select ENSP00000312262.5:n.555+1G>A
NM_001619.3:c.555+1G>A NP_001610.2:n.555+1G>A
NM_001619.4:c.555+1G>A NP_001610.2:n.555+1G>A
ENST00000308595.9:c.555+1G>A ENSP00000312262.5:n.555+1G>A
ENST00000416281.6:n.1178G>A
ENST00000526285.1:c.555+1G>A ENSP00000434126.1:n.555+1G>A
ENST00000529738.1:n.183+884G>A
ENST00000533077.5:n.591G>A
XM_011544773.1:c.465+1G>A XP_011543075.1:n.465+1G>A
XM_024448376.1:c.480+1G>A XP_024304144.1:n.480+1G>A
XR_001747779.1:n.835+1G>A
XR_949796.1:n.855+1G>A