Canonical Allele Identifier: CA2488887552

Gene: ROCK2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11214007A= , CM000664.2:g.11214007A=	GRCh38
NC_000002.11:g.11354133A= , CM000664.1:g.11354133A=	GRCh37
NC_000002.10:g.11271584A=	NCBI36
NG_029769.1:g.135579T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697752.1:c.2043+350T=	ENSP00000513431.1:n.2043+350T=
ENST00000697790.1:c.354+350T=	ENSP00000513442.1:n.354+350T=
ENST00000697791.1:n.2403+350T=
ENST00000697792.1:n.2403+350T=
ENST00000315872.11:c.2043+350T= MANE Select	ENSP00000317985.6:n.2043+350T=
ENST00000315872.10:c.2043+350T=	ENSP00000317985.6:n.2043+350T=
ENST00000401753.5:c.1314+350T=	ENSP00000385509.1:n.1314+350T=
ENST00000616279.4:c.-13+350T=	ENSP00000481789.1:n.-13+350T=
NM_004850.3:c.2043+350T=	NP_004841.2:n.2043+350T=
XM_005246190.3:c.2043+350T=	XP_005246247.1:n.2043+350T=
XM_011510417.1:c.1785+350T=	XP_011508719.1:n.1785+350T=
NM_001321643.1:c.1785+350T=	NP_001308572.1:n.1785+350T=
NM_004850.4:c.2043+350T=	NP_004841.2:n.2043+350T=
XM_011510417.2:c.1785+350T=	XP_011508719.1:n.1785+350T=
XM_017005378.2:c.2043+350T=	XP_016860867.1:n.2043+350T=
XM_017005379.2:c.1785+350T=	XP_016860868.1:n.1785+350T=
NM_004850.5:c.2043+350T= MANE Select	NP_004841.2:n.2043+350T=
NM_001321643.2:c.1785+350T=	NP_001308572.1:n.1785+350T=