Canonical Allele Identifier: CA2123452705
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423430_23423440delinsAACACAAACAC , CM000676.2:g.23423430_23423440delinsAACACAAACAC GRCh38
NC_000014.8:g.23892639_23892649delinsAACACAAACAC , CM000676.1:g.23892639_23892649delinsAACACAAACAC GRCh37
NC_000014.7:g.22962479_22962489delinsAACACAAACAC NCBI36
NG_007884.1:g.17222_17232delinsGTGTTTGTGTT , LRG_384:g.17222_17232delinsGTGTTTGTGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+107_3099+117delinsGTGTTTGTGTT MANE Select ENSP00000347507.3:n.3099+107_3099+117delinsGTGTTTGTGTT
ENST00000355349.3:c.3099+107_3099+117delinsGTGTTTGTGTT ENSP00000347507.3:n.3099+107_3099+117delinsGTGTTTGTGTT
NM_000257.3:c.3099+107_3099+117delinsGTGTTTGTGTT NP_000248.2:n.3099+107_3099+117delinsGTGTTTGTGTT
XR_245686.3:n.3205+107_3205+117delinsGTGTTTGTGTT
XM_017021340.1:c.3099+107_3099+117delinsGTGTTTGTGTT XP_016876829.1:n.3099+107_3099+117delinsGTGTTTGTGTT
NM_000257.4:c.3099+107_3099+117delinsGTGTTTGTGTT MANE Select NP_000248.2:n.3099+107_3099+117delinsGTGTTTGTGTT
Search 100 bp 5'
Search 100 bp 3'