Canonical Allele Identifier: CA2123456101

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433718C= , CM000676.2:g.23433718C=	GRCh38
NC_000014.8:g.23902927C= , CM000676.1:g.23902927C=	GRCh37
NC_000014.7:g.22972767C=	NCBI36
NG_007884.1:g.6944G= , LRG_384:g.6944G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.15G= MANE Select	ENSP00000347507.3:p.Glu5=
ENST00000355349.3:c.15G=	ENSP00000347507.3:p.Glu5=
NM_000257.3:c.15G=	NP_000248.2:p.Glu5=
XR_245686.3:n.121G=
XM_017021340.1:c.15G=	XP_016876829.1:p.Glu5=
NM_000257.4:c.15G= MANE Select	NP_000248.2:p.Glu5=