Canonical Allele Identifier: CA2123456483
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433994_23434006delinsCCCTGTAGGAGCA , CM000676.2:g.23433994_23434006delinsCCCTGTAGGAGCA GRCh38
NC_000014.8:g.23903203_23903215delinsCCCTGTAGGAGCA , CM000676.1:g.23903203_23903215delinsCCCTGTAGGAGCA GRCh37
NC_000014.7:g.22973043_22973055delinsCCCTGTAGGAGCA NCBI36
NG_007884.1:g.6656_6668delinsTGCTCCTACAGGG , LRG_384:g.6656_6668delinsTGCTCCTACAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.-9+188_-9+200delinsTGCTCCTACAGGG MANE Select ENSP00000347507.3:n.-9+188_-9+200delinsTGCTCCTACAGGG
ENST00000355349.3:c.-9+188_-9+200delinsTGCTCCTACAGGG ENSP00000347507.3:n.-9+188_-9+200delinsTGCTCCTACAGGG
NM_000257.3:c.-9+188_-9+200delinsTGCTCCTACAGGG NP_000248.2:n.-9+188_-9+200delinsTGCTCCTACAGGG
XR_245686.3:n.98+188_98+200delinsTGCTCCTACAGGG
XM_017021340.1:c.-8-266_-8-254delinsTGCTCCTACAGGG XP_016876829.1:n.-8-266_-8-254delinsTGCTCCTACAGGG
NM_000257.4:c.-9+188_-9+200delinsTGCTCCTACAGGG MANE Select NP_000248.2:n.-9+188_-9+200delinsTGCTCCTACAGGG
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