Canonical Allele Identifier: CA2123458967
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23413950_23413951delinsTG , CM000676.2:g.23413950_23413951delinsTG GRCh38
NC_000014.8:g.23883159_23883160delinsTG , CM000676.1:g.23883159_23883160delinsTG GRCh37
NC_000014.7:g.22952999_22953000delinsTG NCBI36
NG_007884.1:g.26711_26712delinsCA , LRG_384:g.26711_26712delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5655+56_5656-57delinsCA MANE Select ENSP00000347507.3:n.5655+56_5656-57delinsCA
ENST00000355349.3:c.5655+56_5656-57delinsCA ENSP00000347507.3:n.5655+56_5656-57delinsCA
NM_000257.3:c.5655+56_5656-57delinsCA NP_000248.2:n.5655+56_5656-57delinsCA
XM_017021340.1:c.5655+56_5656-57delinsCA XP_016876829.1:n.5655+56_5656-57delinsCA
NM_000257.4:c.5655+56_5656-57delinsCA MANE Select NP_000248.2:n.5655+56_5656-57delinsCA
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