Canonical Allele Identifier: CA2123451433
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422558_23422576delinsATTCTTTCTTTCTTTCCCT , CM000676.2:g.23422558_23422576delinsATTCTTTCTTTCTTTCCCT GRCh38
NC_000014.8:g.23891767_23891785delinsATTCTTTCTTTCTTTCCCT , CM000676.1:g.23891767_23891785delinsATTCTTTCTTTCTTTCCCT GRCh37
NC_000014.7:g.22961607_22961625delinsATTCTTTCTTTCTTTCCCT NCBI36
NG_007884.1:g.18086_18104delinsAGGGAAAGAAAGAAAGAAT , LRG_384:g.18086_18104delinsAGGGAAAGAAAGAAAGAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3100-251_3100-233delinsAGGGAAAGAAAGAAAGAAT MANE Select ENSP00000347507.3:n.3100-251_3100-233delinsAGGGAAAGAAAGAAAGAA...
ENST00000355349.3:c.3100-251_3100-233delinsAGGGAAAGAAAGAAAGAAT ENSP00000347507.3:n.3100-251_3100-233delinsAGGGAAAGAAAGAAAGAA...
NM_000257.3:c.3100-251_3100-233delinsAGGGAAAGAAAGAAAGAAT NP_000248.2:n.3100-251_3100-233delinsAGGGAAAGAAAGAAAGAAT
XR_245686.3:n.3206-251_3206-233delinsAGGGAAAGAAAGAAAGAAT
XM_017021340.1:c.3100-251_3100-233delinsAGGGAAAGAAAGAAAGAAT XP_016876829.1:n.3100-251_3100-233delinsAGGGAAAGAAAGAAAGAAT
NM_000257.4:c.3100-251_3100-233delinsAGGGAAAGAAAGAAAGAAT MANE Select NP_000248.2:n.3100-251_3100-233delinsAGGGAAAGAAAGAAAGAAT