Canonical Allele Identifier: CA1027558204

Gene: ROCK2

Linked Data

• gnomAD v3: 2-11214212-T-TCGAG
• gnomAD v4: 2-11214212-T-TCGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11214212_11214213insCGAG , CM000664.2:g.11214212_11214213insCGAG	GRCh38
NC_000002.11:g.11354338_11354339insCGAG , CM000664.1:g.11354338_11354339insCGAG	GRCh37
NC_000002.10:g.11271789_11271790insCGAG	NCBI36
NG_029769.1:g.135373_135374insCTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697752.1:c.2043+144_2043+145insCTCG	ENSP00000513431.1:n.2043+144_2043+145insCTCG
ENST00000697790.1:c.354+144_354+145insCTCG	ENSP00000513442.1:n.354+144_354+145insCTCG
ENST00000697791.1:n.2403+144_2403+145insCTCG
ENST00000697792.1:n.2403+144_2403+145insCTCG
ENST00000315872.11:c.2043+144_2043+145insCTCG MANE Select	ENSP00000317985.6:n.2043+144_2043+145insCTCG
ENST00000315872.10:c.2043+144_2043+145insCTCG	ENSP00000317985.6:n.2043+144_2043+145insCTCG
ENST00000401753.5:c.1314+144_1314+145insCTCG	ENSP00000385509.1:n.1314+144_1314+145insCTCG
ENST00000616279.4:c.-13+144_-13+145insCTCG	ENSP00000481789.1:n.-13+144_-13+145insCTCG
NM_004850.3:c.2043+144_2043+145insCTCG	NP_004841.2:n.2043+144_2043+145insCTCG
XM_005246190.3:c.2043+144_2043+145insCTCG	XP_005246247.1:n.2043+144_2043+145insCTCG
XM_011510417.1:c.1785+144_1785+145insCTCG	XP_011508719.1:n.1785+144_1785+145insCTCG
NM_001321643.1:c.1785+144_1785+145insCTCG	NP_001308572.1:n.1785+144_1785+145insCTCG
NM_004850.4:c.2043+144_2043+145insCTCG	NP_004841.2:n.2043+144_2043+145insCTCG
XM_011510417.2:c.1785+144_1785+145insCTCG	XP_011508719.1:n.1785+144_1785+145insCTCG
XM_017005378.2:c.2043+144_2043+145insCTCG	XP_016860867.1:n.2043+144_2043+145insCTCG
XM_017005379.2:c.1785+144_1785+145insCTCG	XP_016860868.1:n.1785+144_1785+145insCTCG
NM_004850.5:c.2043+144_2043+145insCTCG MANE Select	NP_004841.2:n.2043+144_2043+145insCTCG
NM_001321643.2:c.1785+144_1785+145insCTCG	NP_001308572.1:n.1785+144_1785+145insCTCG