Canonical Allele Identifier: CA2488911510
Gene: ROCK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11268831_11268832delinsCG , CM000664.2:g.11268831_11268832delinsCG GRCh38
NC_000002.11:g.11408957_11408958delinsCG , CM000664.1:g.11408957_11408958delinsCG GRCh37
NC_000002.10:g.11326408_11326409delinsCG NCBI36
NG_029769.1:g.80754_80755delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000431087.2:c.183+17707_183+17708delinsCG ENSP00000395957.2:n.183+17707_183+17708delinsCG
ENST00000697752.1:c.324+17707_324+17708delinsCG ENSP00000513431.1:n.324+17707_324+17708delinsCG
ENST00000315872.11:c.324+17707_324+17708delinsCG MANE Select ENSP00000317985.6:n.324+17707_324+17708delinsCG
ENST00000261535.7:c.324+17707_324+17708delinsCG ENSP00000261535.3:n.324+17707_324+17708delinsCG
ENST00000315872.10:c.324+17707_324+17708delinsCG ENSP00000317985.6:n.324+17707_324+17708delinsCG
ENST00000431087.1:c.66+17707_66+17708delinsCG ENSP00000395957.1:n.66+17707_66+17708delinsCG
ENST00000462366.1:n.346+17707_346+17708delinsCG
ENST00000616279.4:c.-1732+17707_-1732+17708delinsCG ENSP00000481789.1:n.-1732+17707_-1732+17708delinsCG
NM_004850.3:c.324+17707_324+17708delinsCG NP_004841.2:n.324+17707_324+17708delinsCG
XM_005246190.3:c.324+17707_324+17708delinsCG XP_005246247.1:n.324+17707_324+17708delinsCG
XM_011510417.1:c.66+17707_66+17708delinsCG XP_011508719.1:n.66+17707_66+17708delinsCG
NM_001321643.1:c.66+17707_66+17708delinsCG NP_001308572.1:n.66+17707_66+17708delinsCG
NM_004850.4:c.324+17707_324+17708delinsCG NP_004841.2:n.324+17707_324+17708delinsCG
XM_011510417.2:c.66+17707_66+17708delinsCG XP_011508719.1:n.66+17707_66+17708delinsCG
XM_017005378.2:c.324+17707_324+17708delinsCG XP_016860867.1:n.324+17707_324+17708delinsCG
XM_017005379.2:c.66+17707_66+17708delinsCG XP_016860868.1:n.66+17707_66+17708delinsCG
NM_004850.5:c.324+17707_324+17708delinsCG MANE Select NP_004841.2:n.324+17707_324+17708delinsCG
NM_001321643.2:c.66+17707_66+17708delinsCG NP_001308572.1:n.66+17707_66+17708delinsCG