Canonical Allele Identifier: CA2624234785

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416314_23416315insC , CM000676.2:g.23416314_23416315insC GRCh38
NC_000014.8:g.23885523_23885524insC , CM000676.1:g.23885523_23885524insC GRCh37
NC_000014.7:g.22955363_22955364insC NCBI36
NG_007884.1:g.24347_24348insG , LRG_384:g.24347_24348insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4645-3_4645-2insG (MYH7) MANE Select ENSP00000347507.3:n.4645-3_4645-2insG
ENST00000355349.3:c.4645-3_4645-2insG (MYH7) ENSP00000347507.3:n.4645-3_4645-2insG
NM_000257.3:c.4645-3_4645-2insG (MYH7) NP_000248.2:n.4645-3_4645-2insG
NR_126491.1:n.558+17_558+18insC (MHRT)
XM_017021340.1:c.4645-3_4645-2insG (MYH7) XP_016876829.1:n.4645-3_4645-2insG
NM_000257.4:c.4645-3_4645-2insG (MYH7) MANE Select NP_000248.2:n.4645-3_4645-2insG