Canonical Allele Identifier: CA2123441143
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417610T= , CM000676.2:g.23417610T= GRCh38
NC_000014.8:g.23886819T= , CM000676.1:g.23886819T= GRCh37
NC_000014.7:g.22956659T= NCBI36
NG_007884.1:g.23052A= , LRG_384:g.23052A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4246A= MANE Select ENSP00000347507.3:p.Lys1416=
ENST00000355349.3:c.4246A= ENSP00000347507.3:p.Lys1416=
NM_000257.3:c.4246A= NP_000248.2:p.Lys1416=
XM_017021340.1:c.4246A= XP_016876829.1:p.Lys1416=
NM_000257.4:c.4246A= MANE Select NP_000248.2:p.Lys1416=