Canonical Allele Identifier: CA1362296538

Gene: MYL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46858418C= , CM000665.2:g.46858418C=	GRCh38
NC_000003.11:g.46899908C= , CM000665.1:g.46899908C=	GRCh37
NC_000003.10:g.46874912C=	NCBI36
NG_007555.2:g.28752G= , LRG_395:g.28752G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000431168.2:c.525G=	ENSP00000393455.2:p.Gly175=
ENST00000292327.6:c.525G= MANE Select	ENSP00000292327.4:p.Gly175=
ENST00000653454.1:c.525G=	ENSP00000499624.1:p.Gly175=
ENST00000654597.1:c.525G=	ENSP00000499406.1:p.Gly175=
ENST00000655244.1:n.732G=
ENST00000662933.1:c.525G=	ENSP00000499577.1:p.Gly175=
ENST00000664891.1:n.483G=
ENST00000292327.4:c.525G=	ENSP00000292327.4:p.Gly175=
ENST00000395869.5:c.525G=	ENSP00000379210.1:p.Gly175=
NM_000258.2:c.525G= , LRG_395t1:c.525G=	NP_000249.1:p.Gly175=
NM_000258.3:c.525G= MANE Select	NP_000249.1:p.Gly175=