Canonical Allele Identifier: CA2401409834
Community Standard Title: NM_005569.4(LIMK2):c.1142G= (p.Arg381=)
Gene: LIMK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.31267789G= , CM000684.2:g.31267789G= GRCh38
NC_000022.10:g.31663775G= , CM000684.1:g.31663775G= GRCh37
NC_000022.9:g.29993775G= NCBI36
NG_029895.1:g.60526G=
NG_029895.2:g.60526G=

Transcript Alleles

HGVS Amino-acid Change
NM_005569.4:c.1142G= MANE Select NP_005560.1:p.Arg381=
ENST00000331728.9:c.1142G= MANE Select ENSP00000332687.4:p.Arg381=
NM_001031801.1:c.1079G= NP_001026971.1:p.Arg360=
NM_001031801.2:c.1079G= NP_001026971.1:p.Arg360=
NM_005569.3:c.1142G= NP_005560.1:p.Arg381=
NM_016733.2:c.1079G= NP_057952.1:p.Arg360=
NM_016733.3:c.1079G= NP_057952.1:p.Arg360=
ENST00000331728.8:c.1142G= ENSP00000332687.4:p.Arg381=
ENST00000333611.8:c.1079G= ENSP00000330470.4:p.Arg360=
ENST00000340552.4:c.1079G= ENSP00000339916.4:p.Arg360=
ENST00000406516.5:c.908G= ENSP00000384602.1:p.Arg303=