Canonical Allele Identifier: CA2123465758

Gene: MYH7 MHRT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23416205T= , CM000676.2:g.23416205T=	GRCh38
NC_000014.8:g.23885414T= , CM000676.1:g.23885414T=	GRCh37
NC_000014.7:g.22955254T=	NCBI36
NG_007884.1:g.24457A= , LRG_384:g.24457A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4752A= (MYH7) MANE Select	ENSP00000347507.3:p.Glu1584=
ENST00000355349.3:c.4752A= (MYH7)	ENSP00000347507.3:p.Glu1584=
NM_000257.3:c.4752A= (MYH7)	NP_000248.2:p.Glu1584=
NR_126491.1:n.466T= (MHRT)
XM_017021340.1:c.4752A= (MYH7)	XP_016876829.1:p.Glu1584=
NM_000257.4:c.4752A= (MYH7) MANE Select	NP_000248.2:p.Glu1584=