Canonical Allele Identifier: CA2624234399
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422256_23422257insTGGGTCAG , CM000676.2:g.23422256_23422257insTGGGTCAG GRCh38
NC_000014.8:g.23891465_23891466insTGGGTCAG , CM000676.1:g.23891465_23891466insTGGGTCAG GRCh37
NC_000014.7:g.22961305_22961306insTGGGTCAG NCBI36
NG_007884.1:g.18405_18406insCTGACCCA , LRG_384:g.18405_18406insCTGACCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3168_3169insCTGACCCA MANE Select ENSP00000347507.3:p.Gly1057LeufsTer6
ENST00000355349.3:c.3168_3169insCTGACCCA ENSP00000347507.3:p.Gly1057LeufsTer6
NM_000257.3:c.3168_3169insCTGACCCA NP_000248.2:p.Gly1057LeufsTer6
XR_245686.3:n.3274_3275insCTGACCCA
XM_017021340.1:c.3168_3169insCTGACCCA XP_016876829.1:p.Gly1057LeufsTer6
NM_000257.4:c.3168_3169insCTGACCCA MANE Select NP_000248.2:p.Gly1057LeufsTer6