Canonical Allele Identifier: CA2123445507
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429094G= , CM000676.2:g.23429094G= GRCh38
NC_000014.8:g.23898303G= , CM000676.1:g.23898303G= GRCh37
NC_000014.7:g.22968143G= NCBI36
NG_007884.1:g.11568C= , LRG_384:g.11568C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1268C= MANE Select ENSP00000347507.3:p.Ala423=
ENST00000355349.3:c.1268C= ENSP00000347507.3:p.Ala423=
NM_000257.3:c.1268C= NP_000248.2:p.Ala423=
XR_245686.3:n.1374C=
XM_017021340.1:c.1268C= XP_016876829.1:p.Ala423=
NM_000257.4:c.1268C= MANE Select NP_000248.2:p.Ala423=