Canonical Allele Identifier: CA1362297682

Gene: MYL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46860806C= , CM000665.2:g.46860806C=	GRCh38
NC_000003.11:g.46902296C= , CM000665.1:g.46902296C=	GRCh37
NC_000003.10:g.46877300C=	NCBI36
NG_007555.2:g.26364G= , LRG_395:g.26364G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.177G=	ENSP00000393455.2:p.Met59=
ENST00000292327.6:c.177G= MANE Select	ENSP00000292327.4:p.Met59=
ENST00000653454.1:c.177G=	ENSP00000499624.1:p.Met59=
ENST00000654597.1:c.177G=	ENSP00000499406.1:p.Met59=
ENST00000655244.1:n.399G=
ENST00000662933.1:c.177G=	ENSP00000499577.1:p.Met59=
ENST00000664891.1:n.135G=
ENST00000292327.4:c.177G=	ENSP00000292327.4:p.Met59=
ENST00000395869.5:c.177G=	ENSP00000379210.1:p.Met59=
NM_000258.2:c.177G= , LRG_395t1:c.177G=	NP_000249.1:p.Met59=
NM_000258.3:c.177G= MANE Select	NP_000249.1:p.Met59=