Canonical Allele Identifier: CA2488911360
Gene: ROCK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11268537_11268538delinsTG , CM000664.2:g.11268537_11268538delinsTG GRCh38
NC_000002.11:g.11408663_11408664delinsTG , CM000664.1:g.11408663_11408664delinsTG GRCh37
NC_000002.10:g.11326114_11326115delinsTG NCBI36
NG_029769.1:g.81048_81049delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000431087.2:c.183+18001_183+18002delinsCA ENSP00000395957.2:n.183+18001_183+18002delinsCA
ENST00000697752.1:c.324+18001_324+18002delinsCA ENSP00000513431.1:n.324+18001_324+18002delinsCA
ENST00000315872.11:c.324+18001_324+18002delinsCA MANE Select ENSP00000317985.6:n.324+18001_324+18002delinsCA
ENST00000261535.7:c.324+18001_324+18002delinsCA ENSP00000261535.3:n.324+18001_324+18002delinsCA
ENST00000315872.10:c.324+18001_324+18002delinsCA ENSP00000317985.6:n.324+18001_324+18002delinsCA
ENST00000431087.1:c.66+18001_66+18002delinsCA ENSP00000395957.1:n.66+18001_66+18002delinsCA
ENST00000462366.1:n.346+18001_346+18002delinsCA
ENST00000616279.4:c.-1732+18001_-1732+18002delinsCA ENSP00000481789.1:n.-1732+18001_-1732+18002delinsCA
NM_004850.3:c.324+18001_324+18002delinsCA NP_004841.2:n.324+18001_324+18002delinsCA
XM_005246190.3:c.324+18001_324+18002delinsCA XP_005246247.1:n.324+18001_324+18002delinsCA
XM_011510417.1:c.66+18001_66+18002delinsCA XP_011508719.1:n.66+18001_66+18002delinsCA
NM_001321643.1:c.66+18001_66+18002delinsCA NP_001308572.1:n.66+18001_66+18002delinsCA
NM_004850.4:c.324+18001_324+18002delinsCA NP_004841.2:n.324+18001_324+18002delinsCA
XM_011510417.2:c.66+18001_66+18002delinsCA XP_011508719.1:n.66+18001_66+18002delinsCA
XM_017005378.2:c.324+18001_324+18002delinsCA XP_016860867.1:n.324+18001_324+18002delinsCA
XM_017005379.2:c.66+18001_66+18002delinsCA XP_016860868.1:n.66+18001_66+18002delinsCA
NM_004850.5:c.324+18001_324+18002delinsCA MANE Select NP_004841.2:n.324+18001_324+18002delinsCA
NM_001321643.2:c.66+18001_66+18002delinsCA NP_001308572.1:n.66+18001_66+18002delinsCA