Canonical Allele Identifier: CA1027571506
Gene: ROCK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11269009_11269010insTAT , CM000664.2:g.11269009_11269010insTAT GRCh38
NC_000002.11:g.11409135_11409136insTAT , CM000664.1:g.11409135_11409136insTAT GRCh37
NC_000002.10:g.11326586_11326587insTAT NCBI36
NG_029769.1:g.80576_80577insATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000431087.2:c.183+17529_183+17530insATA ENSP00000395957.2:n.183+17529_183+17530insATA
ENST00000697752.1:c.324+17529_324+17530insATA ENSP00000513431.1:n.324+17529_324+17530insATA
ENST00000315872.11:c.324+17529_324+17530insATA MANE Select ENSP00000317985.6:n.324+17529_324+17530insATA
ENST00000261535.7:c.324+17529_324+17530insATA ENSP00000261535.3:n.324+17529_324+17530insATA
ENST00000315872.10:c.324+17529_324+17530insATA ENSP00000317985.6:n.324+17529_324+17530insATA
ENST00000431087.1:c.66+17529_66+17530insATA ENSP00000395957.1:n.66+17529_66+17530insATA
ENST00000462366.1:n.346+17529_346+17530insATA
ENST00000616279.4:c.-1732+17529_-1732+17530insATA ENSP00000481789.1:n.-1732+17529_-1732+17530insATA
NM_004850.3:c.324+17529_324+17530insATA NP_004841.2:n.324+17529_324+17530insATA
XM_005246190.3:c.324+17529_324+17530insATA XP_005246247.1:n.324+17529_324+17530insATA
XM_011510417.1:c.66+17529_66+17530insATA XP_011508719.1:n.66+17529_66+17530insATA
NM_001321643.1:c.66+17529_66+17530insATA NP_001308572.1:n.66+17529_66+17530insATA
NM_004850.4:c.324+17529_324+17530insATA NP_004841.2:n.324+17529_324+17530insATA
XM_011510417.2:c.66+17529_66+17530insATA XP_011508719.1:n.66+17529_66+17530insATA
XM_017005378.2:c.324+17529_324+17530insATA XP_016860867.1:n.324+17529_324+17530insATA
XM_017005379.2:c.66+17529_66+17530insATA XP_016860868.1:n.66+17529_66+17530insATA
NM_004850.5:c.324+17529_324+17530insATA MANE Select NP_004841.2:n.324+17529_324+17530insATA
NM_001321643.2:c.66+17529_66+17530insATA NP_001308572.1:n.66+17529_66+17530insATA