Canonical Allele Identifier: CA2624233555
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23421179_23421180insC , CM000676.2:g.23421179_23421180insC GRCh38
NC_000014.8:g.23890388_23890389insC , CM000676.1:g.23890388_23890389insC GRCh37
NC_000014.7:g.22960228_22960229insC NCBI36
NG_007884.1:g.19482_19483insG , LRG_384:g.19482_19483insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3246-132_3246-131insG MANE Select ENSP00000347507.3:n.3246-132_3246-131insG
ENST00000355349.3:c.3246-132_3246-131insG ENSP00000347507.3:n.3246-132_3246-131insG
NM_000257.3:c.3246-132_3246-131insG NP_000248.2:n.3246-132_3246-131insG
XR_245686.3:n.3354-132_3354-131insG
XM_017021340.1:c.3246-132_3246-131insG XP_016876829.1:n.3246-132_3246-131insG
NM_000257.4:c.3246-132_3246-131insG MANE Select NP_000248.2:n.3246-132_3246-131insG