Canonical Allele Identifier: CA2123451317
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422504_23422505delinsCA , CM000676.2:g.23422504_23422505delinsCA GRCh38
NC_000014.8:g.23891713_23891714delinsCA , CM000676.1:g.23891713_23891714delinsCA GRCh37
NC_000014.7:g.22961553_22961554delinsCA NCBI36
NG_007884.1:g.18157_18158delinsTG , LRG_384:g.18157_18158delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3100-180_3100-179delinsTG MANE Select ENSP00000347507.3:n.3100-180_3100-179delinsTG
ENST00000355349.3:c.3100-180_3100-179delinsTG ENSP00000347507.3:n.3100-180_3100-179delinsTG
NM_000257.3:c.3100-180_3100-179delinsTG NP_000248.2:n.3100-180_3100-179delinsTG
XR_245686.3:n.3206-180_3206-179delinsTG
XM_017021340.1:c.3100-180_3100-179delinsTG XP_016876829.1:n.3100-180_3100-179delinsTG
NM_000257.4:c.3100-180_3100-179delinsTG MANE Select NP_000248.2:n.3100-180_3100-179delinsTG