Canonical Allele Identifier: CA2624235292
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423436_23423437insTCACACACAC , CM000676.2:g.23423436_23423437insTCACACACAC GRCh38
NC_000014.8:g.23892645_23892646insTCACACACAC , CM000676.1:g.23892645_23892646insTCACACACAC GRCh37
NC_000014.7:g.22962485_22962486insTCACACACAC NCBI36
NG_007884.1:g.17225_17226insGTGTGTGTGA , LRG_384:g.17225_17226insGTGTGTGTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+110_3099+111insGTGTGTGTGA MANE Select ENSP00000347507.3:n.3099+110_3099+111insGTGTGTGTGA
ENST00000355349.3:c.3099+110_3099+111insGTGTGTGTGA ENSP00000347507.3:n.3099+110_3099+111insGTGTGTGTGA
NM_000257.3:c.3099+110_3099+111insGTGTGTGTGA NP_000248.2:n.3099+110_3099+111insGTGTGTGTGA
XR_245686.3:n.3205+110_3205+111insGTGTGTGTGA
XM_017021340.1:c.3099+110_3099+111insGTGTGTGTGA XP_016876829.1:n.3099+110_3099+111insGTGTGTGTGA
NM_000257.4:c.3099+110_3099+111insGTGTGTGTGA MANE Select NP_000248.2:n.3099+110_3099+111insGTGTGTGTGA