Canonical Allele Identifier: CA2123448012

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420653_23420666delinsTAACAGGGGAGGGC , CM000676.2:g.23420653_23420666delinsTAACAGGGGAGGGC	GRCh38
NC_000014.8:g.23889862_23889875delinsTAACAGGGGAGGGC , CM000676.1:g.23889862_23889875delinsTAACAGGGGAGGGC	GRCh37
NC_000014.7:g.22959702_22959715delinsTAACAGGGGAGGGC	NCBI36
NG_007884.1:g.19996_20009delinsGCCCTCCCCTGTTA , LRG_384:g.19996_20009delinsGCCCTCCCCTGTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3336+292_3336+305delinsGCCCTCCCCTGTTA MANE Select	ENSP00000347507.3:n.3336+292_3336+305delinsGCCCTCCCCTGTTA
ENST00000355349.3:c.3336+292_3336+305delinsGCCCTCCCCTGTTA	ENSP00000347507.3:n.3336+292_3336+305delinsGCCCTCCCCTGTTA
NM_000257.3:c.3336+292_3336+305delinsGCCCTCCCCTGTTA	NP_000248.2:n.3336+292_3336+305delinsGCCCTCCCCTGTTA
XR_245686.3:n.3444+292_3444+305delinsGCCCTCCCCTGTTA
XM_017021340.1:c.3336+292_3336+305delinsGCCCTCCCCTGTTA	XP_016876829.1:n.3336+292_3336+305delinsGCCCTCCCCTGTTA
NM_000257.4:c.3336+292_3336+305delinsGCCCTCCCCTGTTA MANE Select	NP_000248.2:n.3336+292_3336+305delinsGCCCTCCCCTGTTA