Canonical Allele Identifier: CA485626726
Community Standard Title: NM_000257.4(MYH7):c.306C>A (p.Leu102=)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433123G>T , CM000676.2:g.23433123G>T GRCh38
NC_000014.8:g.23902332G>T , CM000676.1:g.23902332G>T GRCh37
NC_000014.7:g.22972172G>T NCBI36
NG_007884.1:g.7539C>A , LRG_384:g.7539C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.306C>A MANE Select NP_000248.2:p.Leu102=
ENST00000355349.4:c.306C>A MANE Select ENSP00000347507.3:p.Leu102=
NM_000257.3:c.306C>A NP_000248.2:p.Leu102=
ENST00000355349.3:c.306C>A ENSP00000347507.3:p.Leu102=
XM_017021340.1:c.306C>A XP_016876829.1:p.Leu102=
XR_245686.3:n.412C>A