Canonical Allele Identifier: CA2652342911
Gene: MYLK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31819980_31819982del , CM000682.2:g.31819980_31819982del GRCh38
NC_000020.10:g.30407783_30407785del , CM000682.1:g.30407783_30407785del GRCh37
NC_000020.9:g.29871444_29871446del NCBI36
NG_012847.1:g.5606_5608del , LRG_392:g.5606_5608del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.53-146_53-144del MANE Select ENSP00000365152.4:n.53-146_53-144del
ENST00000375985.4:c.53-146_53-144del ENSP00000365152.4:n.53-146_53-144del
ENST00000375994.6:c.53-146_53-144del ENSP00000365162.2:n.53-146_53-144del
NM_033118.3:c.53-146_53-144del , LRG_392t1:c.53-146_53-144del NP_149109.1:n.53-146_53-144del
XR_244155.1:n.218-146_218-144del
NM_033118.4:c.53-146_53-144del MANE Select NP_149109.1:n.53-146_53-144del