Canonical Allele Identifier: CA2360015389

Gene: MYLK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.31820158C= , CM000682.2:g.31820158C=	GRCh38
NC_000020.10:g.30407961C= , CM000682.1:g.30407961C=	GRCh37
NC_000020.9:g.29871622C=	NCBI36
NG_012847.1:g.5784C= , LRG_392:g.5784C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375985.5:c.85C= MANE Select	ENSP00000365152.4:p.Pro29=
ENST00000375985.4:c.85C=	ENSP00000365152.4:p.Pro29=
ENST00000375994.6:c.85C=	ENSP00000365162.2:p.Pro29=
NM_033118.3:c.85C= , LRG_392t1:c.85C=	NP_149109.1:p.Pro29=
XR_244155.1:n.250C=
NM_033118.4:c.85C= MANE Select	NP_149109.1:p.Pro29=