Canonical Allele Identifier: CA2123451952
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431583_23431584delinsAC , CM000676.2:g.23431583_23431584delinsAC GRCh38
NC_000014.8:g.23900792_23900793delinsAC , CM000676.1:g.23900792_23900793delinsAC GRCh37
NC_000014.7:g.22970632_22970633delinsAC NCBI36
NG_007884.1:g.9078_9079delinsGT , LRG_384:g.9078_9079delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.732+1_732+2delinsGT MANE Select ENSP00000347507.3:n.732+1_732+2delinsGT
ENST00000355349.3:c.732+1_732+2delinsGT ENSP00000347507.3:n.732+1_732+2delinsGT
NM_000257.3:c.732+1_732+2delinsGT NP_000248.2:n.732+1_732+2delinsGT
XR_245686.3:n.838+1_838+2delinsGT
XM_017021340.1:c.732+1_732+2delinsGT XP_016876829.1:n.732+1_732+2delinsGT
NM_000257.4:c.732+1_732+2delinsGT MANE Select NP_000248.2:n.732+1_732+2delinsGT