Canonical Allele Identifier: CA2123443884

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23428544C= , CM000676.2:g.23428544C=	GRCh38
NC_000014.8:g.23897753C= , CM000676.1:g.23897753C=	GRCh37
NC_000014.7:g.22967593C=	NCBI36
NG_007884.1:g.12118G= , LRG_384:g.12118G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355349.4:c.1534G= MANE Select	ENSP00000347507.3:p.Asp512=
ENST00000355349.3:c.1534G=	ENSP00000347507.3:p.Asp512=
NM_000257.3:c.1534G=	NP_000248.2:p.Asp512=
XR_245686.3:n.1640G=
XM_017021340.1:c.1534G=	XP_016876829.1:p.Asp512=
NM_000257.4:c.1534G= MANE Select	NP_000248.2:p.Asp512=