Canonical Allele Identifier: CA2360017142
Gene: MYLK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.31824295A= , CM000682.2:g.31824295A= GRCh38
NC_000020.10:g.30412098A= , CM000682.1:g.30412098A= GRCh37
NC_000020.9:g.29875759A= NCBI36
NG_012847.1:g.9921A= , LRG_392:g.9921A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375985.5:c.915A= MANE Select ENSP00000365152.4:p.Lys305=
ENST00000375985.4:c.915A= ENSP00000365152.4:p.Lys305=
ENST00000375994.6:c.915A= ENSP00000365162.2:p.Lys305=
NM_033118.3:c.915A= , LRG_392t1:c.915A= NP_149109.1:p.Lys305=
XR_244155.1:n.1281A=
NM_033118.4:c.915A= MANE Select NP_149109.1:p.Lys305=