Canonical Allele Identifier: CA2748862841
Gene: ROCK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11268532_11268533insAG , CM000664.2:g.11268532_11268533insAG GRCh38
NC_000002.11:g.11408658_11408659insAG , CM000664.1:g.11408658_11408659insAG GRCh37
NC_000002.10:g.11326109_11326110insAG NCBI36
NG_029769.1:g.81054_81055insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000431087.2:c.183+18007_183+18008insTC ENSP00000395957.2:n.183+18007_183+18008insTC
ENST00000697752.1:c.324+18007_324+18008insTC ENSP00000513431.1:n.324+18007_324+18008insTC
ENST00000315872.11:c.324+18007_324+18008insTC MANE Select ENSP00000317985.6:n.324+18007_324+18008insTC
ENST00000261535.7:c.324+18007_324+18008insTC ENSP00000261535.3:n.324+18007_324+18008insTC
ENST00000315872.10:c.324+18007_324+18008insTC ENSP00000317985.6:n.324+18007_324+18008insTC
ENST00000431087.1:c.66+18007_66+18008insTC ENSP00000395957.1:n.66+18007_66+18008insTC
ENST00000462366.1:n.346+18007_346+18008insTC
ENST00000616279.4:c.-1732+18007_-1732+18008insTC ENSP00000481789.1:n.-1732+18007_-1732+18008insTC
NM_004850.3:c.324+18007_324+18008insTC NP_004841.2:n.324+18007_324+18008insTC
XM_005246190.3:c.324+18007_324+18008insTC XP_005246247.1:n.324+18007_324+18008insTC
XM_011510417.1:c.66+18007_66+18008insTC XP_011508719.1:n.66+18007_66+18008insTC
NM_001321643.1:c.66+18007_66+18008insTC NP_001308572.1:n.66+18007_66+18008insTC
NM_004850.4:c.324+18007_324+18008insTC NP_004841.2:n.324+18007_324+18008insTC
XM_011510417.2:c.66+18007_66+18008insTC XP_011508719.1:n.66+18007_66+18008insTC
XM_017005378.2:c.324+18007_324+18008insTC XP_016860867.1:n.324+18007_324+18008insTC
XM_017005379.2:c.66+18007_66+18008insTC XP_016860868.1:n.66+18007_66+18008insTC
NM_004850.5:c.324+18007_324+18008insTC MANE Select NP_004841.2:n.324+18007_324+18008insTC
NM_001321643.2:c.66+18007_66+18008insTC NP_001308572.1:n.66+18007_66+18008insTC