Canonical Allele Identifier: CA2488889539

Gene: ROCK2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11218994G= , CM000664.2:g.11218994G=	GRCh38
NC_000002.11:g.11359120G= , CM000664.1:g.11359120G=	GRCh37
NC_000002.10:g.11276571G=	NCBI36
NG_029769.1:g.130592C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004850.5:c.1292C= MANE Select	NP_004841.2:p.Thr431=
ENST00000315872.11:c.1292C= MANE Select	ENSP00000317985.6:p.Thr431=
NM_001321643.1:c.1034C=	NP_001308572.1:p.Thr345=
NM_001321643.2:c.1034C=	NP_001308572.1:p.Thr345=
NM_004850.3:c.1292C=	NP_004841.2:p.Thr431=
NM_004850.4:c.1292C=	NP_004841.2:p.Thr431=
ENST00000261535.7:c.1292C=	ENSP00000261535.3:p.Thr431=
ENST00000315872.10:c.1292C=	ENSP00000317985.6:p.Thr431=
ENST00000401753.5:c.563C=	ENSP00000385509.1:p.Thr188=
ENST00000484951.1:n.176C=
ENST00000616279.4:c.-764C=	ENSP00000481789.1:n.-764C=
ENST00000697752.1:c.1292C=	ENSP00000513431.1:p.Thr431=
ENST00000697791.1:n.333C=
ENST00000697792.1:n.333C=
XM_005246190.3:c.1292C=	XP_005246247.1:p.Thr431=
XM_011510417.1:c.1034C=	XP_011508719.1:p.Thr345=
XM_011510417.2:c.1034C=	XP_011508719.1:p.Thr345=
XM_017005378.2:c.1292C=	XP_016860867.1:p.Thr431=
XM_017005379.2:c.1034C=	XP_016860868.1:p.Thr345=