Canonical Allele Identifier: CA2624235408
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423441_23423442insAACA , CM000676.2:g.23423441_23423442insAACA GRCh38
NC_000014.8:g.23892650_23892651insAACA , CM000676.1:g.23892650_23892651insAACA GRCh37
NC_000014.7:g.22962490_22962491insAACA NCBI36
NG_007884.1:g.17223_17224insTTGT , LRG_384:g.17223_17224insTTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+108_3099+109insTTGT MANE Select ENSP00000347507.3:n.3099+108_3099+109insTTGT
ENST00000355349.3:c.3099+108_3099+109insTTGT ENSP00000347507.3:n.3099+108_3099+109insTTGT
NM_000257.3:c.3099+108_3099+109insTTGT NP_000248.2:n.3099+108_3099+109insTTGT
XR_245686.3:n.3205+108_3205+109insTTGT
XM_017021340.1:c.3099+108_3099+109insTTGT XP_016876829.1:n.3099+108_3099+109insTTGT
NM_000257.4:c.3099+108_3099+109insTTGT MANE Select NP_000248.2:n.3099+108_3099+109insTTGT