Canonical Allele Identifier: CA2624235313
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423441_23423442insAACACACACA , CM000676.2:g.23423441_23423442insAACACACACA GRCh38
NC_000014.8:g.23892650_23892651insAACACACACA , CM000676.1:g.23892650_23892651insAACACACACA GRCh37
NC_000014.7:g.22962490_22962491insAACACACACA NCBI36
NG_007884.1:g.17225_17226insGTGTTTGTGT , LRG_384:g.17225_17226insGTGTTTGTGT

Transcript Alleles

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