Canonical Allele Identifier: CA2624232733
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420870_23420871insTC , CM000676.2:g.23420870_23420871insTC GRCh38
NC_000014.8:g.23890079_23890080insTC , CM000676.1:g.23890079_23890080insTC GRCh37
NC_000014.7:g.22959919_22959920insTC NCBI36
NG_007884.1:g.19791_19792insGA , LRG_384:g.19791_19792insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+87_3336+88insGA MANE Select ENSP00000347507.3:n.3336+87_3336+88insGA
ENST00000355349.3:c.3336+87_3336+88insGA ENSP00000347507.3:n.3336+87_3336+88insGA
NM_000257.3:c.3336+87_3336+88insGA NP_000248.2:n.3336+87_3336+88insGA
XR_245686.3:n.3444+87_3444+88insGA
XM_017021340.1:c.3336+87_3336+88insGA XP_016876829.1:n.3336+87_3336+88insGA
NM_000257.4:c.3336+87_3336+88insGA MANE Select NP_000248.2:n.3336+87_3336+88insGA