Canonical Allele Identifier: CA389053126
Community Standard Title: NM_000257.4(MYH7):c.311A>T (p.Asn104Ile)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433118T>A , CM000676.2:g.23433118T>A GRCh38
NC_000014.8:g.23902327T>A , CM000676.1:g.23902327T>A GRCh37
NC_000014.7:g.22972167T>A NCBI36
NG_007884.1:g.7544A>T , LRG_384:g.7544A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.311A>T MANE Select NP_000248.2:p.Asn104Ile
ENST00000355349.4:c.311A>T MANE Select ENSP00000347507.3:p.Asn104Ile
NM_000257.3:c.311A>T NP_000248.2:p.Asn104Ile
ENST00000355349.3:c.311A>T ENSP00000347507.3:p.Asn104Ile
XM_017021340.1:c.311A>T XP_016876829.1:p.Asn104Ile
XR_245686.3:n.417A>T