Canonical Allele Identifier: CA389053148
Community Standard Title: NM_000257.4(MYH7):c.305T>G (p.Leu102Arg)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433124A>C , CM000676.2:g.23433124A>C GRCh38
NC_000014.8:g.23902333A>C , CM000676.1:g.23902333A>C GRCh37
NC_000014.7:g.22972173A>C NCBI36
NG_007884.1:g.7538T>G , LRG_384:g.7538T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.305T>G MANE Select NP_000248.2:p.Leu102Arg
ENST00000355349.4:c.305T>G MANE Select ENSP00000347507.3:p.Leu102Arg
NM_000257.3:c.305T>G NP_000248.2:p.Leu102Arg
ENST00000355349.3:c.305T>G ENSP00000347507.3:p.Leu102Arg
XM_017021340.1:c.305T>G XP_016876829.1:p.Leu102Arg
XR_245686.3:n.411T>G