Canonical Allele Identifier: CA2624235598
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423478_23423479insCCAC , CM000676.2:g.23423478_23423479insCCAC GRCh38
NC_000014.8:g.23892687_23892688insCCAC , CM000676.1:g.23892687_23892688insCCAC GRCh37
NC_000014.7:g.22962527_22962528insCCAC NCBI36
NG_007884.1:g.17186_17187insGGTG , LRG_384:g.17186_17187insGGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+71_3099+72insGGTG MANE Select ENSP00000347507.3:n.3099+71_3099+72insGGTG
ENST00000355349.3:c.3099+71_3099+72insGGTG ENSP00000347507.3:n.3099+71_3099+72insGGTG
NM_000257.3:c.3099+71_3099+72insGGTG NP_000248.2:n.3099+71_3099+72insGGTG
XR_245686.3:n.3205+71_3205+72insGGTG
XM_017021340.1:c.3099+71_3099+72insGGTG XP_016876829.1:n.3099+71_3099+72insGGTG
NM_000257.4:c.3099+71_3099+72insGGTG MANE Select NP_000248.2:n.3099+71_3099+72insGGTG