Canonical Allele Identifier: CA2123442973

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23418385C= , CM000676.2:g.23418385C=	GRCh38
NC_000014.8:g.23887594C= , CM000676.1:g.23887594C=	GRCh37
NC_000014.7:g.22957434C=	NCBI36
NG_007884.1:g.22277G= , LRG_384:g.22277G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3994G= MANE Select	ENSP00000347507.3:p.Ala1332=
ENST00000355349.3:c.3994G=	ENSP00000347507.3:p.Ala1332=
NM_000257.3:c.3994G=	NP_000248.2:p.Ala1332=
XM_017021340.1:c.3994G=	XP_016876829.1:p.Ala1332=
NM_000257.4:c.3994G= MANE Select	NP_000248.2:p.Ala1332=