Canonical Allele Identifier: CA2624234907

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416330_23416342del , CM000676.2:g.23416330_23416342del GRCh38
NC_000014.8:g.23885539_23885551del , CM000676.1:g.23885539_23885551del GRCh37
NC_000014.7:g.22955379_22955391del NCBI36
NG_007884.1:g.24322_24334del , LRG_384:g.24322_24334del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4645-28_4645-16del (MYH7) MANE Select ENSP00000347507.3:n.4645-28_4645-16del
ENST00000355349.3:c.4645-28_4645-16del (MYH7) ENSP00000347507.3:n.4645-28_4645-16del
NM_000257.3:c.4645-28_4645-16del (MYH7) NP_000248.2:n.4645-28_4645-16del
NR_126491.1:n.558+33_558+45del (MHRT)
XM_017021340.1:c.4645-28_4645-16del (MYH7) XP_016876829.1:n.4645-28_4645-16del
NM_000257.4:c.4645-28_4645-16del (MYH7) MANE Select NP_000248.2:n.4645-28_4645-16del