Canonical Allele Identifier: CA2123453312
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423656T= , CM000676.2:g.23423656T= GRCh38
NC_000014.8:g.23892865T= , CM000676.1:g.23892865T= GRCh37
NC_000014.7:g.22962705T= NCBI36
NG_007884.1:g.17006A= , LRG_384:g.17006A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2990A= MANE Select ENSP00000347507.3:p.Lys997=
ENST00000355349.3:c.2990A= ENSP00000347507.3:p.Lys997=
NM_000257.3:c.2990A= NP_000248.2:p.Lys997=
XR_245686.3:n.3096A=
XM_017021340.1:c.2990A= XP_016876829.1:p.Lys997=
NM_000257.4:c.2990A= MANE Select NP_000248.2:p.Lys997=