Canonical Allele Identifier: CA2123456229

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23424921C= , CM000676.2:g.23424921C=	GRCh38
NC_000014.8:g.23894130C= , CM000676.1:g.23894130C=	GRCh37
NC_000014.7:g.22963970C=	NCBI36
NG_007884.1:g.15741G= , LRG_384:g.15741G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2527G= MANE Select	ENSP00000347507.3:p.Ala843=
ENST00000355349.3:c.2527G=	ENSP00000347507.3:p.Ala843=
NM_000257.3:c.2527G=	NP_000248.2:p.Ala843=
XR_245686.3:n.2633G=
XM_017021340.1:c.2527G=	XP_016876829.1:p.Ala843=
NM_000257.4:c.2527G= MANE Select	NP_000248.2:p.Ala843=