Canonical Allele Identifier: CA2488911371

Gene: ROCK2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11268546G= , CM000664.2:g.11268546G=	GRCh38
NC_000002.11:g.11408672G= , CM000664.1:g.11408672G=	GRCh37
NC_000002.10:g.11326123G=	NCBI36
NG_029769.1:g.81040C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431087.2:c.183+17993C=	ENSP00000395957.2:n.183+17993C=
ENST00000697752.1:c.324+17993C=	ENSP00000513431.1:n.324+17993C=
ENST00000315872.11:c.324+17993C= MANE Select	ENSP00000317985.6:n.324+17993C=
ENST00000261535.7:c.324+17993C=	ENSP00000261535.3:n.324+17993C=
ENST00000315872.10:c.324+17993C=	ENSP00000317985.6:n.324+17993C=
ENST00000431087.1:c.66+17993C=	ENSP00000395957.1:n.66+17993C=
ENST00000462366.1:n.346+17993C=
ENST00000616279.4:c.-1732+17993C=	ENSP00000481789.1:n.-1732+17993C=
NM_004850.3:c.324+17993C=	NP_004841.2:n.324+17993C=
XM_005246190.3:c.324+17993C=	XP_005246247.1:n.324+17993C=
XM_011510417.1:c.66+17993C=	XP_011508719.1:n.66+17993C=
NM_001321643.1:c.66+17993C=	NP_001308572.1:n.66+17993C=
NM_004850.4:c.324+17993C=	NP_004841.2:n.324+17993C=
XM_011510417.2:c.66+17993C=	XP_011508719.1:n.66+17993C=
XM_017005378.2:c.324+17993C=	XP_016860867.1:n.324+17993C=
XM_017005379.2:c.66+17993C=	XP_016860868.1:n.66+17993C=
NM_004850.5:c.324+17993C= MANE Select	NP_004841.2:n.324+17993C=
NM_001321643.2:c.66+17993C=	NP_001308572.1:n.66+17993C=