Canonical Allele Identifier: CA2123468485

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417288C= , CM000676.2:g.23417288C= GRCh38
NC_000014.8:g.23886497C= , CM000676.1:g.23886497C= GRCh37
NC_000014.7:g.22956337C= NCBI36
NG_007884.1:g.23374G= , LRG_384:g.23374G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4384G= (MYH7) MANE Select ENSP00000347507.3:p.Glu1462=
ENST00000355349.3:c.4384G= (MYH7) ENSP00000347507.3:p.Glu1462=
NM_000257.3:c.4384G= (MYH7) NP_000248.2:p.Glu1462=
NR_126491.1:n.728C= (MHRT)
XM_017021340.1:c.4384G= (MYH7) XP_016876829.1:p.Glu1462=
NM_000257.4:c.4384G= (MYH7) MANE Select NP_000248.2:p.Glu1462=