Canonical Allele Identifier: CA2575504411
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423487_23423488insT , CM000676.2:g.23423487_23423488insT GRCh38
NC_000014.8:g.23892696_23892697insT , CM000676.1:g.23892696_23892697insT GRCh37
NC_000014.7:g.22962536_22962537insT NCBI36
NG_007884.1:g.17174_17175insA , LRG_384:g.17174_17175insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+59_3099+60insA MANE Select ENSP00000347507.3:n.3099+59_3099+60insA
ENST00000355349.3:c.3099+59_3099+60insA ENSP00000347507.3:n.3099+59_3099+60insA
NM_000257.3:c.3099+59_3099+60insA NP_000248.2:n.3099+59_3099+60insA
XR_245686.3:n.3205+59_3205+60insA
XM_017021340.1:c.3099+59_3099+60insA XP_016876829.1:n.3099+59_3099+60insA
NM_000257.4:c.3099+59_3099+60insA MANE Select NP_000248.2:n.3099+59_3099+60insA