Canonical Allele Identifier: CA2123452749
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431824_23431825delinsGA , CM000676.2:g.23431824_23431825delinsGA GRCh38
NC_000014.8:g.23901033_23901034delinsGA , CM000676.1:g.23901033_23901034delinsGA GRCh37
NC_000014.7:g.22970873_22970874delinsGA NCBI36
NG_007884.1:g.8837_8838delinsTC , LRG_384:g.8837_8838delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.575_576delinsTC MANE Select ENSP00000347507.3:p.Ile192=
ENST00000355349.3:c.575_576delinsTC ENSP00000347507.3:p.Ile192=
NM_000257.3:c.575_576delinsTC NP_000248.2:p.Ile192=
XR_245686.3:n.681_682delinsTC
XM_017021340.1:c.575_576delinsTC XP_016876829.1:p.Ile192=
NM_000257.4:c.575_576delinsTC MANE Select NP_000248.2:p.Ile192=