Canonical Allele Identifier: CA2123457992

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23425605T= , CM000676.2:g.23425605T=	GRCh38
NC_000014.8:g.23894814T= , CM000676.1:g.23894814T=	GRCh37
NC_000014.7:g.22964654T=	NCBI36
NG_007884.1:g.15057A= , LRG_384:g.15057A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2286+90A= MANE Select	ENSP00000347507.3:n.2286+90A=
ENST00000355349.3:c.2286+90A=	ENSP00000347507.3:n.2286+90A=
NM_000257.3:c.2286+90A=	NP_000248.2:n.2286+90A=
XR_245686.3:n.2392+90A=
XM_017021340.1:c.2286+90A=	XP_016876829.1:n.2286+90A=
NM_000257.4:c.2286+90A= MANE Select	NP_000248.2:n.2286+90A=