Canonical Allele Identifier: CA2123449232

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23421317T= , CM000676.2:g.23421317T=	GRCh38
NC_000014.8:g.23890526T= , CM000676.1:g.23890526T=	GRCh37
NC_000014.7:g.22960366T=	NCBI36
NG_007884.1:g.19345A= , LRG_384:g.19345A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3246-269A= MANE Select	ENSP00000347507.3:n.3246-269A=
ENST00000355349.3:c.3246-269A=	ENSP00000347507.3:n.3246-269A=
NM_000257.3:c.3246-269A=	NP_000248.2:n.3246-269A=
XR_245686.3:n.3354-269A=
XM_017021340.1:c.3246-269A=	XP_016876829.1:n.3246-269A=
NM_000257.4:c.3246-269A= MANE Select	NP_000248.2:n.3246-269A=