Canonical Allele Identifier: CA2573149779
Community Standard Title: NM_000257.4(MYH7):c.4035_4036delinsAA (p.Gln1346Lys)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23418343_23418344delinsTT , CM000676.2:g.23418343_23418344delinsTT GRCh38
NC_000014.8:g.23887552_23887553delinsTT , CM000676.1:g.23887552_23887553delinsTT GRCh37
NC_000014.7:g.22957392_22957393delinsTT NCBI36
NG_007884.1:g.22318_22319delinsAA , LRG_384:g.22318_22319delinsAA

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.4035_4036delinsAA MANE Select NP_000248.2:p.Gln1346Lys
ENST00000355349.4:c.4035_4036delinsAA MANE Select ENSP00000347507.3:p.Gln1346Lys
NM_000257.3:c.4035_4036delinsAA NP_000248.2:p.Gln1346Lys
ENST00000355349.3:c.4035_4036delinsAA ENSP00000347507.3:p.Gln1346Lys
XM_017021340.1:c.4035_4036delinsAA XP_016876829.1:p.Gln1346Lys