Canonical Allele Identifier: CA1362297618

Gene: MYL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46860681T= , CM000665.2:g.46860681T=	GRCh38
NC_000003.11:g.46902171T= , CM000665.1:g.46902171T=	GRCh37
NC_000003.10:g.46877175T=	NCBI36
NG_007555.2:g.26489A= , LRG_395:g.26489A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.302A=	ENSP00000393455.2:p.Gln101=
ENST00000292327.6:c.302A= MANE Select	ENSP00000292327.4:p.Gln101=
ENST00000653454.1:c.302A=	ENSP00000499624.1:p.Gln101=
ENST00000654597.1:c.302A=	ENSP00000499406.1:p.Gln101=
ENST00000655244.1:n.524A=
ENST00000662933.1:c.302A=	ENSP00000499577.1:p.Gln101=
ENST00000664891.1:n.260A=
ENST00000292327.4:c.302A=	ENSP00000292327.4:p.Gln101=
ENST00000395869.5:c.302A=	ENSP00000379210.1:p.Gln101=
NM_000258.2:c.302A= , LRG_395t1:c.302A=	NP_000249.1:p.Gln101=
NM_000258.3:c.302A= MANE Select	NP_000249.1:p.Gln101=