Canonical Allele Identifier: CA2123452779
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431833_23431834delinsCT , CM000676.2:g.23431833_23431834delinsCT GRCh38
NC_000014.8:g.23901042_23901043delinsCT , CM000676.1:g.23901042_23901043delinsCT GRCh37
NC_000014.7:g.22970882_22970883delinsCT NCBI36
NG_007884.1:g.8828_8829delinsAG , LRG_384:g.8828_8829delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.566_567delinsAG MANE Select ENSP00000347507.3:p.Lys189=
ENST00000355349.3:c.566_567delinsAG ENSP00000347507.3:p.Lys189=
NM_000257.3:c.566_567delinsAG NP_000248.2:p.Lys189=
XR_245686.3:n.672_673delinsAG
XM_017021340.1:c.566_567delinsAG XP_016876829.1:p.Lys189=
NM_000257.4:c.566_567delinsAG MANE Select NP_000248.2:p.Lys189=