Canonical Allele Identifier: CA2123451425
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422558_23422562delinsATTCT , CM000676.2:g.23422558_23422562delinsATTCT GRCh38
NC_000014.8:g.23891767_23891771delinsATTCT , CM000676.1:g.23891767_23891771delinsATTCT GRCh37
NC_000014.7:g.22961607_22961611delinsATTCT NCBI36
NG_007884.1:g.18100_18104delinsAGAAT , LRG_384:g.18100_18104delinsAGAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3100-237_3100-233delinsAGAAT MANE Select ENSP00000347507.3:n.3100-237_3100-233delinsAGAAT
ENST00000355349.3:c.3100-237_3100-233delinsAGAAT ENSP00000347507.3:n.3100-237_3100-233delinsAGAAT
NM_000257.3:c.3100-237_3100-233delinsAGAAT NP_000248.2:n.3100-237_3100-233delinsAGAAT
XR_245686.3:n.3206-237_3206-233delinsAGAAT
XM_017021340.1:c.3100-237_3100-233delinsAGAAT XP_016876829.1:n.3100-237_3100-233delinsAGAAT
NM_000257.4:c.3100-237_3100-233delinsAGAAT MANE Select NP_000248.2:n.3100-237_3100-233delinsAGAAT