Canonical Allele Identifier: CA2123451336
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422522_23422530delinsGGAATAAAT , CM000676.2:g.23422522_23422530delinsGGAATAAAT GRCh38
NC_000014.8:g.23891731_23891739delinsGGAATAAAT , CM000676.1:g.23891731_23891739delinsGGAATAAAT GRCh37
NC_000014.7:g.22961571_22961579delinsGGAATAAAT NCBI36
NG_007884.1:g.18132_18140delinsATTTATTCC , LRG_384:g.18132_18140delinsATTTATTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3100-205_3100-197delinsATTTATTCC MANE Select ENSP00000347507.3:n.3100-205_3100-197delinsATTTATTCC
ENST00000355349.3:c.3100-205_3100-197delinsATTTATTCC ENSP00000347507.3:n.3100-205_3100-197delinsATTTATTCC
NM_000257.3:c.3100-205_3100-197delinsATTTATTCC NP_000248.2:n.3100-205_3100-197delinsATTTATTCC
XR_245686.3:n.3206-205_3206-197delinsATTTATTCC
XM_017021340.1:c.3100-205_3100-197delinsATTTATTCC XP_016876829.1:n.3100-205_3100-197delinsATTTATTCC
NM_000257.4:c.3100-205_3100-197delinsATTTATTCC MANE Select NP_000248.2:n.3100-205_3100-197delinsATTTATTCC
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