Canonical Allele Identifier: CA2563778702
Gene: ROCK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11268560_11268561insACCTA , CM000664.2:g.11268560_11268561insACCTA GRCh38
NC_000002.11:g.11408686_11408687insACCTA , CM000664.1:g.11408686_11408687insACCTA GRCh37
NC_000002.10:g.11326137_11326138insACCTA NCBI36
NG_029769.1:g.81025_81026insTAGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000431087.2:c.183+17978_183+17979insTAGGT ENSP00000395957.2:n.183+17978_183+17979insTAGGT
ENST00000697752.1:c.324+17978_324+17979insTAGGT ENSP00000513431.1:n.324+17978_324+17979insTAGGT
ENST00000315872.11:c.324+17978_324+17979insTAGGT MANE Select ENSP00000317985.6:n.324+17978_324+17979insTAGGT
ENST00000261535.7:c.324+17978_324+17979insTAGGT ENSP00000261535.3:n.324+17978_324+17979insTAGGT
ENST00000315872.10:c.324+17978_324+17979insTAGGT ENSP00000317985.6:n.324+17978_324+17979insTAGGT
ENST00000431087.1:c.66+17978_66+17979insTAGGT ENSP00000395957.1:n.66+17978_66+17979insTAGGT
ENST00000462366.1:n.346+17978_346+17979insTAGGT
ENST00000616279.4:c.-1732+17978_-1732+17979insTAGGT ENSP00000481789.1:n.-1732+17978_-1732+17979insTAGGT
NM_004850.3:c.324+17978_324+17979insTAGGT NP_004841.2:n.324+17978_324+17979insTAGGT
XM_005246190.3:c.324+17978_324+17979insTAGGT XP_005246247.1:n.324+17978_324+17979insTAGGT
XM_011510417.1:c.66+17978_66+17979insTAGGT XP_011508719.1:n.66+17978_66+17979insTAGGT
NM_001321643.1:c.66+17978_66+17979insTAGGT NP_001308572.1:n.66+17978_66+17979insTAGGT
NM_004850.4:c.324+17978_324+17979insTAGGT NP_004841.2:n.324+17978_324+17979insTAGGT
XM_011510417.2:c.66+17978_66+17979insTAGGT XP_011508719.1:n.66+17978_66+17979insTAGGT
XM_017005378.2:c.324+17978_324+17979insTAGGT XP_016860867.1:n.324+17978_324+17979insTAGGT
XM_017005379.2:c.66+17978_66+17979insTAGGT XP_016860868.1:n.66+17978_66+17979insTAGGT
NM_004850.5:c.324+17978_324+17979insTAGGT MANE Select NP_004841.2:n.324+17978_324+17979insTAGGT
NM_001321643.2:c.66+17978_66+17979insTAGGT NP_001308572.1:n.66+17978_66+17979insTAGGT