Canonical Allele Identifier: CA1362297098

Gene: MYL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46859518G= , CM000665.2:g.46859518G=	GRCh38
NC_000003.11:g.46901008G= , CM000665.1:g.46901008G=	GRCh37
NC_000003.10:g.46876012G=	NCBI36
NG_007555.2:g.27652C= , LRG_395:g.27652C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.438C=	ENSP00000393455.2:p.Gly146=
ENST00000292327.6:c.438C= MANE Select	ENSP00000292327.4:p.Gly146=
ENST00000653454.1:c.438C=	ENSP00000499624.1:p.Gly146=
ENST00000654597.1:c.438C=	ENSP00000499406.1:p.Gly146=
ENST00000655244.1:n.660C=
ENST00000662933.1:c.438C=	ENSP00000499577.1:p.Gly146=
ENST00000664891.1:n.396C=
ENST00000292327.4:c.438C=	ENSP00000292327.4:p.Gly146=
ENST00000395869.5:c.438C=	ENSP00000379210.1:p.Gly146=
NM_000258.2:c.438C= , LRG_395t1:c.438C=	NP_000249.1:p.Gly146=
NM_000258.3:c.438C= MANE Select	NP_000249.1:p.Gly146=