Canonical Allele Identifier: CA2800863172

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416334_23416335insC , CM000676.2:g.23416334_23416335insC GRCh38
NC_000014.8:g.23885543_23885544insC , CM000676.1:g.23885543_23885544insC GRCh37
NC_000014.7:g.22955383_22955384insC NCBI36
NG_007884.1:g.24327_24328insG , LRG_384:g.24327_24328insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4645-23_4645-22insG (MYH7) MANE Select ENSP00000347507.3:n.4645-23_4645-22insG
ENST00000355349.3:c.4645-23_4645-22insG (MYH7) ENSP00000347507.3:n.4645-23_4645-22insG
NM_000257.3:c.4645-23_4645-22insG (MYH7) NP_000248.2:n.4645-23_4645-22insG
NR_126491.1:n.558+37_558+38insC (MHRT)
XM_017021340.1:c.4645-23_4645-22insG (MYH7) XP_016876829.1:n.4645-23_4645-22insG
NM_000257.4:c.4645-23_4645-22insG (MYH7) MANE Select NP_000248.2:n.4645-23_4645-22insG