Canonical Allele Identifier: CA2624234796

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416318_23416319insCTGC , CM000676.2:g.23416318_23416319insCTGC GRCh38
NC_000014.8:g.23885527_23885528insCTGC , CM000676.1:g.23885527_23885528insCTGC GRCh37
NC_000014.7:g.22955367_22955368insCTGC NCBI36
NG_007884.1:g.24343_24344insGCAG , LRG_384:g.24343_24344insGCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4645-7_4645-6insGCAG (MYH7) MANE Select ENSP00000347507.3:n.4645-7_4645-6insGCAG
ENST00000355349.3:c.4645-7_4645-6insGCAG (MYH7) ENSP00000347507.3:n.4645-7_4645-6insGCAG
NM_000257.3:c.4645-7_4645-6insGCAG (MYH7) NP_000248.2:n.4645-7_4645-6insGCAG
NR_126491.1:n.558+21_558+22insCTGC (MHRT)
XM_017021340.1:c.4645-7_4645-6insGCAG (MYH7) XP_016876829.1:n.4645-7_4645-6insGCAG
NM_000257.4:c.4645-7_4645-6insGCAG (MYH7) MANE Select NP_000248.2:n.4645-7_4645-6insGCAG