Canonical Allele Identifier: CA2534288386
Gene: ROCK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11214091_11214092del , CM000664.2:g.11214091_11214092del GRCh38
NC_000002.11:g.11354217_11354218del , CM000664.1:g.11354217_11354218del GRCh37
NC_000002.10:g.11271668_11271669del NCBI36
NG_029769.1:g.135494_135495del

Transcript Alleles

HGVS Amino-acid change
ENST00000697752.1:c.2043+265_2043+266del ENSP00000513431.1:n.2043+265_2043+266del
ENST00000697790.1:c.354+265_354+266del ENSP00000513442.1:n.354+265_354+266del
ENST00000697791.1:n.2403+265_2403+266del
ENST00000697792.1:n.2403+265_2403+266del
ENST00000315872.11:c.2043+265_2043+266del MANE Select ENSP00000317985.6:n.2043+265_2043+266del
ENST00000315872.10:c.2043+265_2043+266del ENSP00000317985.6:n.2043+265_2043+266del
ENST00000401753.5:c.1314+265_1314+266del ENSP00000385509.1:n.1314+265_1314+266del
ENST00000616279.4:c.-13+265_-13+266del ENSP00000481789.1:n.-13+265_-13+266del
NM_004850.3:c.2043+265_2043+266del NP_004841.2:n.2043+265_2043+266del
XM_005246190.3:c.2043+265_2043+266del XP_005246247.1:n.2043+265_2043+266del
XM_011510417.1:c.1785+265_1785+266del XP_011508719.1:n.1785+265_1785+266del
NM_001321643.1:c.1785+265_1785+266del NP_001308572.1:n.1785+265_1785+266del
NM_004850.4:c.2043+265_2043+266del NP_004841.2:n.2043+265_2043+266del
XM_011510417.2:c.1785+265_1785+266del XP_011508719.1:n.1785+265_1785+266del
XM_017005378.2:c.2043+265_2043+266del XP_016860867.1:n.2043+265_2043+266del
XM_017005379.2:c.1785+265_1785+266del XP_016860868.1:n.1785+265_1785+266del
NM_004850.5:c.2043+265_2043+266del MANE Select NP_004841.2:n.2043+265_2043+266del
NM_001321643.2:c.1785+265_1785+266del NP_001308572.1:n.1785+265_1785+266del