Canonical Allele Identifier: CA1362297689

Gene: MYL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46860816T= , CM000665.2:g.46860816T=	GRCh38
NC_000003.11:g.46902306T= , CM000665.1:g.46902306T=	GRCh37
NC_000003.10:g.46877310T=	NCBI36
NG_007555.2:g.26354A= , LRG_395:g.26354A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.167A=	ENSP00000393455.2:p.Glu56=
ENST00000292327.6:c.167A= MANE Select	ENSP00000292327.4:p.Glu56=
ENST00000653454.1:c.167A=	ENSP00000499624.1:p.Glu56=
ENST00000654597.1:c.167A=	ENSP00000499406.1:p.Glu56=
ENST00000655244.1:n.389A=
ENST00000662933.1:c.167A=	ENSP00000499577.1:p.Glu56=
ENST00000664891.1:n.125A=
ENST00000292327.4:c.167A=	ENSP00000292327.4:p.Glu56=
ENST00000395869.5:c.167A=	ENSP00000379210.1:p.Glu56=
NM_000258.2:c.167A= , LRG_395t1:c.167A=	NP_000249.1:p.Glu56=
NM_000258.3:c.167A= MANE Select	NP_000249.1:p.Glu56=