Canonical Allele Identifier: CA2624235683
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423485_23423489dup , CM000676.2:g.23423485_23423489dup GRCh38
NC_000014.8:g.23892694_23892698dup , CM000676.1:g.23892694_23892698dup GRCh37
NC_000014.7:g.22962534_22962538dup NCBI36
NG_007884.1:g.17173_17177dup , LRG_384:g.17173_17177dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+58_3099+62dup MANE Select ENSP00000347507.3:n.3099+58_3099+62dup
ENST00000355349.3:c.3099+58_3099+62dup ENSP00000347507.3:n.3099+58_3099+62dup
NM_000257.3:c.3099+58_3099+62dup NP_000248.2:n.3099+58_3099+62dup
XR_245686.3:n.3205+58_3205+62dup
XM_017021340.1:c.3099+58_3099+62dup XP_016876829.1:n.3099+58_3099+62dup
NM_000257.4:c.3099+58_3099+62dup MANE Select NP_000248.2:n.3099+58_3099+62dup