Canonical Allele Identifier: CA2123448305
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420819_23420820delinsCT , CM000676.2:g.23420819_23420820delinsCT GRCh38
NC_000014.8:g.23890028_23890029delinsCT , CM000676.1:g.23890028_23890029delinsCT GRCh37
NC_000014.7:g.22959868_22959869delinsCT NCBI36
NG_007884.1:g.19842_19843delinsAG , LRG_384:g.19842_19843delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+138_3336+139delinsAG MANE Select ENSP00000347507.3:n.3336+138_3336+139delinsAG
ENST00000355349.3:c.3336+138_3336+139delinsAG ENSP00000347507.3:n.3336+138_3336+139delinsAG
NM_000257.3:c.3336+138_3336+139delinsAG NP_000248.2:n.3336+138_3336+139delinsAG
XR_245686.3:n.3444+138_3444+139delinsAG
XM_017021340.1:c.3336+138_3336+139delinsAG XP_016876829.1:n.3336+138_3336+139delinsAG
NM_000257.4:c.3336+138_3336+139delinsAG MANE Select NP_000248.2:n.3336+138_3336+139delinsAG