Canonical Allele Identifier: CA2624251032
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431335_23431340del , CM000676.2:g.23431335_23431340del GRCh38
NC_000014.8:g.23900544_23900549del , CM000676.1:g.23900544_23900549del GRCh37
NC_000014.7:g.22970384_22970389del NCBI36
NG_007884.1:g.9322_9327del , LRG_384:g.9322_9327del

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.796+78_796+83del MANE Select ENSP00000347507.3:n.796+78_796+83del
ENST00000355349.3:c.796+78_796+83del ENSP00000347507.3:n.796+78_796+83del
NM_000257.3:c.796+78_796+83del NP_000248.2:n.796+78_796+83del
XR_245686.3:n.902+78_902+83del
XM_017021340.1:c.796+78_796+83del XP_016876829.1:n.796+78_796+83del
NM_000257.4:c.796+78_796+83del MANE Select NP_000248.2:n.796+78_796+83del