Canonical Allele Identifier: CA2624251007
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431316_23431318del , CM000676.2:g.23431316_23431318del GRCh38
NC_000014.8:g.23900525_23900527del , CM000676.1:g.23900525_23900527del GRCh37
NC_000014.7:g.22970365_22970367del NCBI36
NG_007884.1:g.9347_9349del , LRG_384:g.9347_9349del

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.796+103_796+105del MANE Select ENSP00000347507.3:n.796+103_796+105del
ENST00000355349.3:c.796+103_796+105del ENSP00000347507.3:n.796+103_796+105del
NM_000257.3:c.796+103_796+105del NP_000248.2:n.796+103_796+105del
XR_245686.3:n.902+103_902+105del
XM_017021340.1:c.796+103_796+105del XP_016876829.1:n.796+103_796+105del
NM_000257.4:c.796+103_796+105del MANE Select NP_000248.2:n.796+103_796+105del