Canonical Allele Identifier: CA2123452694
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423428_23423434delinsTAAACAC , CM000676.2:g.23423428_23423434delinsTAAACAC GRCh38
NC_000014.8:g.23892637_23892643delinsTAAACAC , CM000676.1:g.23892637_23892643delinsTAAACAC GRCh37
NC_000014.7:g.22962477_22962483delinsTAAACAC NCBI36
NG_007884.1:g.17228_17234delinsGTGTTTA , LRG_384:g.17228_17234delinsGTGTTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+113_3099+119delinsGTGTTTA MANE Select ENSP00000347507.3:n.3099+113_3099+119delinsGTGTTTA
ENST00000355349.3:c.3099+113_3099+119delinsGTGTTTA ENSP00000347507.3:n.3099+113_3099+119delinsGTGTTTA
NM_000257.3:c.3099+113_3099+119delinsGTGTTTA NP_000248.2:n.3099+113_3099+119delinsGTGTTTA
XR_245686.3:n.3205+113_3205+119delinsGTGTTTA
XM_017021340.1:c.3099+113_3099+119delinsGTGTTTA XP_016876829.1:n.3099+113_3099+119delinsGTGTTTA
NM_000257.4:c.3099+113_3099+119delinsGTGTTTA MANE Select NP_000248.2:n.3099+113_3099+119delinsGTGTTTA
Search 100 bp 5'
Search 100 bp 3'