Canonical Allele Identifier: CA2123457094
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23425206_23425207delinsGC , CM000676.2:g.23425206_23425207delinsGC GRCh38
NC_000014.8:g.23894415_23894416delinsGC , CM000676.1:g.23894415_23894416delinsGC GRCh37
NC_000014.7:g.22964255_22964256delinsGC NCBI36
NG_007884.1:g.15455_15456delinsGC , LRG_384:g.15455_15456delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2423+75_2423+76delinsGC MANE Select ENSP00000347507.3:n.2423+75_2423+76delinsGC
ENST00000355349.3:c.2423+75_2423+76delinsGC ENSP00000347507.3:n.2423+75_2423+76delinsGC
NM_000257.3:c.2423+75_2423+76delinsGC NP_000248.2:n.2423+75_2423+76delinsGC
XR_245686.3:n.2529+75_2529+76delinsGC
XM_017021340.1:c.2423+75_2423+76delinsGC XP_016876829.1:n.2423+75_2423+76delinsGC
NM_000257.4:c.2423+75_2423+76delinsGC MANE Select NP_000248.2:n.2423+75_2423+76delinsGC