Canonical Allele Identifier: CA2748862842
Gene: ROCK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11268536_11268537insGGTG , CM000664.2:g.11268536_11268537insGGTG GRCh38
NC_000002.11:g.11408662_11408663insGGTG , CM000664.1:g.11408662_11408663insGGTG GRCh37
NC_000002.10:g.11326113_11326114insGGTG NCBI36
NG_029769.1:g.81052_81053insCCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000431087.2:c.183+18005_183+18006insCCAC ENSP00000395957.2:n.183+18005_183+18006insCCAC
ENST00000697752.1:c.324+18005_324+18006insCCAC ENSP00000513431.1:n.324+18005_324+18006insCCAC
ENST00000315872.11:c.324+18005_324+18006insCCAC MANE Select ENSP00000317985.6:n.324+18005_324+18006insCCAC
ENST00000261535.7:c.324+18005_324+18006insCCAC ENSP00000261535.3:n.324+18005_324+18006insCCAC
ENST00000315872.10:c.324+18005_324+18006insCCAC ENSP00000317985.6:n.324+18005_324+18006insCCAC
ENST00000431087.1:c.66+18005_66+18006insCCAC ENSP00000395957.1:n.66+18005_66+18006insCCAC
ENST00000462366.1:n.346+18005_346+18006insCCAC
ENST00000616279.4:c.-1732+18005_-1732+18006insCCAC ENSP00000481789.1:n.-1732+18005_-1732+18006insCCAC
NM_004850.3:c.324+18005_324+18006insCCAC NP_004841.2:n.324+18005_324+18006insCCAC
XM_005246190.3:c.324+18005_324+18006insCCAC XP_005246247.1:n.324+18005_324+18006insCCAC
XM_011510417.1:c.66+18005_66+18006insCCAC XP_011508719.1:n.66+18005_66+18006insCCAC
NM_001321643.1:c.66+18005_66+18006insCCAC NP_001308572.1:n.66+18005_66+18006insCCAC
NM_004850.4:c.324+18005_324+18006insCCAC NP_004841.2:n.324+18005_324+18006insCCAC
XM_011510417.2:c.66+18005_66+18006insCCAC XP_011508719.1:n.66+18005_66+18006insCCAC
XM_017005378.2:c.324+18005_324+18006insCCAC XP_016860867.1:n.324+18005_324+18006insCCAC
XM_017005379.2:c.66+18005_66+18006insCCAC XP_016860868.1:n.66+18005_66+18006insCCAC
NM_004850.5:c.324+18005_324+18006insCCAC MANE Select NP_004841.2:n.324+18005_324+18006insCCAC
NM_001321643.2:c.66+18005_66+18006insCCAC NP_001308572.1:n.66+18005_66+18006insCCAC