Canonical Allele Identifier: CA2123441893
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23427672G= , CM000676.2:g.23427672G= GRCh38
NC_000014.8:g.23896881G= , CM000676.1:g.23896881G= GRCh37
NC_000014.7:g.22966721G= NCBI36
NG_007884.1:g.12990C= , LRG_384:g.12990C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1801C= MANE Select ENSP00000347507.3:p.Leu601=
ENST00000355349.3:c.1801C= ENSP00000347507.3:p.Leu601=
NM_000257.3:c.1801C= NP_000248.2:p.Leu601=
XR_245686.3:n.1907C=
XM_017021340.1:c.1801C= XP_016876829.1:p.Leu601=
NM_000257.4:c.1801C= MANE Select NP_000248.2:p.Leu601=