Canonical Allele Identifier: CA531052002

Gene: ROCK2

Linked Data

• dbSNP Id: rs1219801391
• gnomAD v2: 2-11409053-CCT-C
• gnomAD v3: 2-11268927-CCT-C
• gnomAD v4: 2-11268927-CCT-C
• MyVariant Identifiers: chr2:g.11409054_11409055del (hg19) ; chr2:g.11268928_11268929del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11268928_11268929del , CM000664.2:g.11268928_11268929del	GRCh38
NC_000002.11:g.11409054_11409055del , CM000664.1:g.11409054_11409055del	GRCh37
NC_000002.10:g.11326505_11326506del	NCBI36
NG_029769.1:g.80657_80658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431087.2:c.183+17610_183+17611del	ENSP00000395957.2:n.183+17610_183+17611del
ENST00000697752.1:c.324+17610_324+17611del	ENSP00000513431.1:n.324+17610_324+17611del
ENST00000315872.11:c.324+17610_324+17611del MANE Select	ENSP00000317985.6:n.324+17610_324+17611del
ENST00000261535.7:c.324+17610_324+17611del	ENSP00000261535.3:n.324+17610_324+17611del
ENST00000315872.10:c.324+17610_324+17611del	ENSP00000317985.6:n.324+17610_324+17611del
ENST00000431087.1:c.66+17610_66+17611del	ENSP00000395957.1:n.66+17610_66+17611del
ENST00000462366.1:n.346+17610_346+17611del
ENST00000616279.4:c.-1732+17610_-1732+17611del	ENSP00000481789.1:n.-1732+17610_-1732+17611del
NM_004850.3:c.324+17610_324+17611del	NP_004841.2:n.324+17610_324+17611del
XM_005246190.3:c.324+17610_324+17611del	XP_005246247.1:n.324+17610_324+17611del
XM_011510417.1:c.66+17610_66+17611del	XP_011508719.1:n.66+17610_66+17611del
NM_001321643.1:c.66+17610_66+17611del	NP_001308572.1:n.66+17610_66+17611del
NM_004850.4:c.324+17610_324+17611del	NP_004841.2:n.324+17610_324+17611del
XM_011510417.2:c.66+17610_66+17611del	XP_011508719.1:n.66+17610_66+17611del
XM_017005378.2:c.324+17610_324+17611del	XP_016860867.1:n.324+17610_324+17611del
XM_017005379.2:c.66+17610_66+17611del	XP_016860868.1:n.66+17610_66+17611del
NM_004850.5:c.324+17610_324+17611del MANE Select	NP_004841.2:n.324+17610_324+17611del
NM_001321643.2:c.66+17610_66+17611del	NP_001308572.1:n.66+17610_66+17611del