Canonical Allele Identifier: CA2123445328
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429040G= , CM000676.2:g.23429040G= GRCh38
NC_000014.8:g.23898249G= , CM000676.1:g.23898249G= GRCh37
NC_000014.7:g.22968089G= NCBI36
NG_007884.1:g.11622C= , LRG_384:g.11622C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1322C= MANE Select ENSP00000347507.3:p.Thr441=
ENST00000355349.3:c.1322C= ENSP00000347507.3:p.Thr441=
NM_000257.3:c.1322C= NP_000248.2:p.Thr441=
XR_245686.3:n.1428C=
XM_017021340.1:c.1322C= XP_016876829.1:p.Thr441=
NM_000257.4:c.1322C= MANE Select NP_000248.2:p.Thr441=