Canonical Allele Identifier: CA2123445428
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429071C= , CM000676.2:g.23429071C= GRCh38
NC_000014.8:g.23898280C= , CM000676.1:g.23898280C= GRCh37
NC_000014.7:g.22968120C= NCBI36
NG_007884.1:g.11591G= , LRG_384:g.11591G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1291G= MANE Select ENSP00000347507.3:p.Val431=
ENST00000355349.3:c.1291G= ENSP00000347507.3:p.Val431=
NM_000257.3:c.1291G= NP_000248.2:p.Val431=
XR_245686.3:n.1397G=
XM_017021340.1:c.1291G= XP_016876829.1:p.Val431=
NM_000257.4:c.1291G= MANE Select NP_000248.2:p.Val431=