Canonical Allele Identifier: CA2123446088
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429286G= , CM000676.2:g.23429286G= GRCh38
NC_000014.8:g.23898495G= , CM000676.1:g.23898495G= GRCh37
NC_000014.7:g.22968335G= NCBI36
NG_007884.1:g.11376C= , LRG_384:g.11376C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1200C= MANE Select ENSP00000347507.3:p.Cys400=
ENST00000355349.3:c.1200C= ENSP00000347507.3:p.Cys400=
NM_000257.3:c.1200C= NP_000248.2:p.Cys400=
XR_245686.3:n.1306C=
XM_017021340.1:c.1200C= XP_016876829.1:p.Cys400=
NM_000257.4:c.1200C= MANE Select NP_000248.2:p.Cys400=