Canonical Allele Identifier: CA2800863173
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416336_23416337insCTACAAG , CM000676.2:g.23416336_23416337insCTACAAG GRCh38
NC_000014.8:g.23885545_23885546insCTACAAG , CM000676.1:g.23885545_23885546insCTACAAG GRCh37
NC_000014.7:g.22955385_22955386insCTACAAG NCBI36
NG_007884.1:g.24325_24326insCTTGTAG , LRG_384:g.24325_24326insCTTGTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4645-25_4645-24insCTTGTAG (MYH7) MANE Select ENSP00000347507.3:n.4645-25_4645-24insCTTGTAG
ENST00000355349.3:c.4645-25_4645-24insCTTGTAG (MYH7) ENSP00000347507.3:n.4645-25_4645-24insCTTGTAG
NM_000257.3:c.4645-25_4645-24insCTTGTAG (MYH7) NP_000248.2:n.4645-25_4645-24insCTTGTAG
NR_126491.1:n.558+39_558+40insCTACAAG (MHRT)
XM_017021340.1:c.4645-25_4645-24insCTTGTAG (MYH7) XP_016876829.1:n.4645-25_4645-24insCTTGTAG
NM_000257.4:c.4645-25_4645-24insCTTGTAG (MYH7) MANE Select NP_000248.2:n.4645-25_4645-24insCTTGTAG
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