Canonical Allele Identifier: CA10190635
Gene: LIMK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.31267889G>A , CM000684.2:g.31267889G>A GRCh38
NC_000022.10:g.31663875G>A , CM000684.1:g.31663875G>A GRCh37
NC_000022.9:g.29993875G>A NCBI36
NG_029895.1:g.60626G>A
NG_029895.2:g.60626G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331728.9:c.1242G>A MANE Select ENSP00000332687.4:p.Lys414=
ENST00000331728.8:c.1242G>A ENSP00000332687.4:p.Lys414=
ENST00000333611.8:c.1179G>A ENSP00000330470.4:p.Lys393=
ENST00000340552.4:c.1179G>A ENSP00000339916.4:p.Lys393=
ENST00000406516.5:c.1008G>A ENSP00000384602.1:p.Lys336=
NM_001031801.1:c.1179G>A NP_001026971.1:p.Lys393=
NM_005569.3:c.1242G>A NP_005560.1:p.Lys414=
NM_016733.2:c.1179G>A NP_057952.1:p.Lys393=
NM_005569.4:c.1242G>A MANE Select NP_005560.1:p.Lys414=
NM_001031801.2:c.1179G>A NP_001026971.1:p.Lys393=
NM_016733.3:c.1179G>A NP_057952.1:p.Lys393=