Canonical Allele Identifier: CA257818592
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs36134932

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423428dup , CM000676.2:g.23423428dup GRCh38
NC_000014.8:g.23892637dup , CM000676.1:g.23892637dup GRCh37
NC_000014.7:g.22962477dup NCBI36
NG_007884.1:g.17234dup , LRG_384:g.17234dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+119dup MANE Select ENSP00000347507.3:n.3099+119dup
ENST00000355349.3:c.3099+119dup ENSP00000347507.3:n.3099+119dup
NM_000257.3:c.3099+119dup NP_000248.2:n.3099+119dup
XR_245686.3:n.3205+119dup
XM_017021340.1:c.3099+119dup XP_016876829.1:n.3099+119dup
NM_000257.4:c.3099+119dup MANE Select NP_000248.2:n.3099+119dup