Canonical Allele Identifier: CA2123452909
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423491_23423496delinsCTCTGG , CM000676.2:g.23423491_23423496delinsCTCTGG GRCh38
NC_000014.8:g.23892700_23892705delinsCTCTGG , CM000676.1:g.23892700_23892705delinsCTCTGG GRCh37
NC_000014.7:g.22962540_22962545delinsCTCTGG NCBI36
NG_007884.1:g.17166_17171delinsCCAGAG , LRG_384:g.17166_17171delinsCCAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+51_3099+56delinsCCAGAG MANE Select ENSP00000347507.3:n.3099+51_3099+56delinsCCAGAG
ENST00000355349.3:c.3099+51_3099+56delinsCCAGAG ENSP00000347507.3:n.3099+51_3099+56delinsCCAGAG
NM_000257.3:c.3099+51_3099+56delinsCCAGAG NP_000248.2:n.3099+51_3099+56delinsCCAGAG
XR_245686.3:n.3205+51_3205+56delinsCCAGAG
XM_017021340.1:c.3099+51_3099+56delinsCCAGAG XP_016876829.1:n.3099+51_3099+56delinsCCAGAG
NM_000257.4:c.3099+51_3099+56delinsCCAGAG MANE Select NP_000248.2:n.3099+51_3099+56delinsCCAGAG