Canonical Allele Identifier: CA389053165
Community Standard Title: NM_000257.4(MYH7):c.301G>A (p.Val101Met)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433128C>T , CM000676.2:g.23433128C>T GRCh38
NC_000014.8:g.23902337C>T , CM000676.1:g.23902337C>T GRCh37
NC_000014.7:g.22972177C>T NCBI36
NG_007884.1:g.7534G>A , LRG_384:g.7534G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.301G>A MANE Select NP_000248.2:p.Val101Met
ENST00000355349.4:c.301G>A MANE Select ENSP00000347507.3:p.Val101Met
NM_000257.3:c.301G>A NP_000248.2:p.Val101Met
ENST00000355349.3:c.301G>A ENSP00000347507.3:p.Val101Met
XM_017021340.1:c.301G>A XP_016876829.1:p.Val101Met
XR_245686.3:n.407G>A