Canonical Allele Identifier: CA2488911317
Gene: ROCK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11268494_11268522delinsGTGTGTGTGTGTATTTAACAGTTTTGCAC , CM000664.2:g.11268494_11268522delinsGTGTGTGTGTGTATTTAACAGTTTTGCAC GRCh38
NC_000002.11:g.11408620_11408648delinsGTGTGTGTGTGTATTTAACAGTTTTGCAC , CM000664.1:g.11408620_11408648delinsGTGTGTGTGTGTATTTAACAGTTTTGCAC GRCh37
NC_000002.10:g.11326071_11326099delinsGTGTGTGTGTGTATTTAACAGTTTTGCAC NCBI36
NG_029769.1:g.81064_81092delinsGTGCAAAACTGTTAAATACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000431087.2:c.183+18017_183+18045delinsGTGCAAAACTGTTAAATACACACACACAC ENSP00000395957.2:n.183+18017_183+18045delinsGTGCAAAACTGTTAAA...
ENST00000697752.1:c.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACACACACAC ENSP00000513431.1:n.324+18017_324+18045delinsGTGCAAAACTGTTAAA...
ENST00000315872.11:c.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACACACACAC MANE Select ENSP00000317985.6:n.324+18017_324+18045delinsGTGCAAAACTGTTAAA...
ENST00000261535.7:c.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACACACACAC ENSP00000261535.3:n.324+18017_324+18045delinsGTGCAAAACTGTTAAA...
ENST00000315872.10:c.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACACACACAC ENSP00000317985.6:n.324+18017_324+18045delinsGTGCAAAACTGTTAAA...
ENST00000431087.1:c.66+18017_66+18045delinsGTGCAAAACTGTTAAATACACACACACAC ENSP00000395957.1:n.66+18017_66+18045delinsGTGCAAAACTGTTAAATA...
ENST00000462366.1:n.346+18017_346+18045delinsGTGCAAAACTGTTAAATACACACACACAC
ENST00000616279.4:c.-1732+18017_-1732+18045delinsGTGCAAAACTGTTAAATACACACACACAC ENSP00000481789.1:n.-1732+18017_-1732+18045delinsGTGCAAAACTGT...
NM_004850.3:c.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACACACACAC NP_004841.2:n.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACA...
XM_005246190.3:c.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACACACACAC XP_005246247.1:n.324+18017_324+18045delinsGTGCAAAACTGTTAAATAC...
XM_011510417.1:c.66+18017_66+18045delinsGTGCAAAACTGTTAAATACACACACACAC XP_011508719.1:n.66+18017_66+18045delinsGTGCAAAACTGTTAAATACAC...
NM_001321643.1:c.66+18017_66+18045delinsGTGCAAAACTGTTAAATACACACACACAC NP_001308572.1:n.66+18017_66+18045delinsGTGCAAAACTGTTAAATACAC...
NM_004850.4:c.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACACACACAC NP_004841.2:n.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACA...
XM_011510417.2:c.66+18017_66+18045delinsGTGCAAAACTGTTAAATACACACACACAC XP_011508719.1:n.66+18017_66+18045delinsGTGCAAAACTGTTAAATACAC...
XM_017005378.2:c.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACACACACAC XP_016860867.1:n.324+18017_324+18045delinsGTGCAAAACTGTTAAATAC...
XM_017005379.2:c.66+18017_66+18045delinsGTGCAAAACTGTTAAATACACACACACAC XP_016860868.1:n.66+18017_66+18045delinsGTGCAAAACTGTTAAATACAC...
NM_004850.5:c.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACACACACAC MANE Select NP_004841.2:n.324+18017_324+18045delinsGTGCAAAACTGTTAAATACACA...
NM_001321643.2:c.66+18017_66+18045delinsGTGCAAAACTGTTAAATACACACACACAC NP_001308572.1:n.66+18017_66+18045delinsGTGCAAAACTGTTAAATACAC...