Canonical Allele Identifier: CA2575486750
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431335_23431338del , CM000676.2:g.23431335_23431338del GRCh38
NC_000014.8:g.23900544_23900547del , CM000676.1:g.23900544_23900547del GRCh37
NC_000014.7:g.22970384_22970387del NCBI36
NG_007884.1:g.9333_9336del , LRG_384:g.9333_9336del

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.796+89_796+92del MANE Select ENSP00000347507.3:n.796+89_796+92del
ENST00000355349.3:c.796+89_796+92del ENSP00000347507.3:n.796+89_796+92del
NM_000257.3:c.796+89_796+92del NP_000248.2:n.796+89_796+92del
XR_245686.3:n.902+89_902+92del
XM_017021340.1:c.796+89_796+92del XP_016876829.1:n.796+89_796+92del
NM_000257.4:c.796+89_796+92del MANE Select NP_000248.2:n.796+89_796+92del