Canonical Allele Identifier: CA2123441851

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417853_23417868delinsGCAGGGCGTGGAGACC , CM000676.2:g.23417853_23417868delinsGCAGGGCGTGGAGACC	GRCh38
NC_000014.8:g.23887062_23887077delinsGCAGGGCGTGGAGACC , CM000676.1:g.23887062_23887077delinsGCAGGGCGTGGAGACC	GRCh37
NC_000014.7:g.22956902_22956917delinsGCAGGGCGTGGAGACC	NCBI36
NG_007884.1:g.22794_22809delinsGGTCTCCACGCCCTGC , LRG_384:g.22794_22809delinsGGTCTCCACGCCCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4170-182_4170-167delinsGGTCTCCACGCCCTGC MANE Select	ENSP00000347507.3:n.4170-182_4170-167delinsGGTCTCCACGCCCTGC
ENST00000355349.3:c.4170-182_4170-167delinsGGTCTCCACGCCCTGC	ENSP00000347507.3:n.4170-182_4170-167delinsGGTCTCCACGCCCTGC
NM_000257.3:c.4170-182_4170-167delinsGGTCTCCACGCCCTGC	NP_000248.2:n.4170-182_4170-167delinsGGTCTCCACGCCCTGC
XM_017021340.1:c.4170-182_4170-167delinsGGTCTCCACGCCCTGC	XP_016876829.1:n.4170-182_4170-167delinsGGTCTCCACGCCCTGC
NM_000257.4:c.4170-182_4170-167delinsGGTCTCCACGCCCTGC MANE Select	NP_000248.2:n.4170-182_4170-167delinsGGTCTCCACGCCCTGC