Canonical Allele Identifier: CA42749341

Gene: ROCK2

Linked Data

• dbSNP Id: rs142209937
• MyVariant Identifiers: chr2:g.11408658_11408659insGT (hg19) ; chr2:g.11268532_11268533insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11268532_11268533insGT , CM000664.2:g.11268532_11268533insGT	GRCh38
NC_000002.11:g.11408658_11408659insGT , CM000664.1:g.11408658_11408659insGT	GRCh37
NC_000002.10:g.11326109_11326110insGT	NCBI36
NG_029769.1:g.81053_81054insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431087.2:c.183+18006_183+18007insAC	ENSP00000395957.2:n.183+18006_183+18007insAC
ENST00000697752.1:c.324+18006_324+18007insAC	ENSP00000513431.1:n.324+18006_324+18007insAC
ENST00000315872.11:c.324+18006_324+18007insAC MANE Select	ENSP00000317985.6:n.324+18006_324+18007insAC
ENST00000261535.7:c.324+18006_324+18007insAC	ENSP00000261535.3:n.324+18006_324+18007insAC
ENST00000315872.10:c.324+18006_324+18007insAC	ENSP00000317985.6:n.324+18006_324+18007insAC
ENST00000431087.1:c.66+18006_66+18007insAC	ENSP00000395957.1:n.66+18006_66+18007insAC
ENST00000462366.1:n.346+18006_346+18007insAC
ENST00000616279.4:c.-1732+18006_-1732+18007insAC	ENSP00000481789.1:n.-1732+18006_-1732+18007insAC
NM_004850.3:c.324+18006_324+18007insAC	NP_004841.2:n.324+18006_324+18007insAC
XM_005246190.3:c.324+18006_324+18007insAC	XP_005246247.1:n.324+18006_324+18007insAC
XM_011510417.1:c.66+18006_66+18007insAC	XP_011508719.1:n.66+18006_66+18007insAC
NM_001321643.1:c.66+18006_66+18007insAC	NP_001308572.1:n.66+18006_66+18007insAC
NM_004850.4:c.324+18006_324+18007insAC	NP_004841.2:n.324+18006_324+18007insAC
XM_011510417.2:c.66+18006_66+18007insAC	XP_011508719.1:n.66+18006_66+18007insAC
XM_017005378.2:c.324+18006_324+18007insAC	XP_016860867.1:n.324+18006_324+18007insAC
XM_017005379.2:c.66+18006_66+18007insAC	XP_016860868.1:n.66+18006_66+18007insAC
NM_004850.5:c.324+18006_324+18007insAC MANE Select	NP_004841.2:n.324+18006_324+18007insAC
NM_001321643.2:c.66+18006_66+18007insAC	NP_001308572.1:n.66+18006_66+18007insAC