Canonical Allele Identifier: CA42523118

Gene: ROCK2

Linked Data

• dbSNP Id: rs961681211
• MyVariant Identifiers: chr2:g.11354219del (hg19) ; chr2:g.11214093del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11214094del , CM000664.2:g.11214094del	GRCh38
NC_000002.11:g.11354220del , CM000664.1:g.11354220del	GRCh37
NC_000002.10:g.11271671del	NCBI36
NG_029769.1:g.135493del

Transcript Alleles

HGVS	Amino-acid change
ENST00000697752.1:c.2043+264del	ENSP00000513431.1:n.2043+264del
ENST00000697790.1:c.354+264del	ENSP00000513442.1:n.354+264del
ENST00000697791.1:n.2403+264del
ENST00000697792.1:n.2403+264del
ENST00000315872.11:c.2043+264del MANE Select	ENSP00000317985.6:n.2043+264del
ENST00000315872.10:c.2043+264del	ENSP00000317985.6:n.2043+264del
ENST00000401753.5:c.1314+264del	ENSP00000385509.1:n.1314+264del
ENST00000616279.4:c.-13+264del	ENSP00000481789.1:n.-13+264del
NM_004850.3:c.2043+264del	NP_004841.2:n.2043+264del
XM_005246190.3:c.2043+264del	XP_005246247.1:n.2043+264del
XM_011510417.1:c.1785+264del	XP_011508719.1:n.1785+264del
NM_001321643.1:c.1785+264del	NP_001308572.1:n.1785+264del
NM_004850.4:c.2043+264del	NP_004841.2:n.2043+264del
XM_011510417.2:c.1785+264del	XP_011508719.1:n.1785+264del
XM_017005378.2:c.2043+264del	XP_016860867.1:n.2043+264del
XM_017005379.2:c.1785+264del	XP_016860868.1:n.1785+264del
NM_004850.5:c.2043+264del MANE Select	NP_004841.2:n.2043+264del
NM_001321643.2:c.1785+264del	NP_001308572.1:n.1785+264del