Canonical Allele Identifier: CA2123452987
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431878_23431893delinsACAGGGGCTTATTGGG , CM000676.2:g.23431878_23431893delinsACAGGGGCTTATTGGG GRCh38
NC_000014.8:g.23901087_23901102delinsACAGGGGCTTATTGGG , CM000676.1:g.23901087_23901102delinsACAGGGGCTTATTGGG GRCh37
NC_000014.7:g.22970927_22970942delinsACAGGGGCTTATTGGG NCBI36
NG_007884.1:g.8769_8784delinsCCCAATAAGCCCCTGT , LRG_384:g.8769_8784delinsCCCAATAAGCCCCTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.531-24_531-9delinsCCCAATAAGCCCCTGT MANE Select ENSP00000347507.3:n.531-24_531-9delinsCCCAATAAGCCCCTGT
ENST00000355349.3:c.531-24_531-9delinsCCCAATAAGCCCCTGT ENSP00000347507.3:n.531-24_531-9delinsCCCAATAAGCCCCTGT
NM_000257.3:c.531-24_531-9delinsCCCAATAAGCCCCTGT NP_000248.2:n.531-24_531-9delinsCCCAATAAGCCCCTGT
XR_245686.3:n.637-24_637-9delinsCCCAATAAGCCCCTGT
XM_017021340.1:c.531-24_531-9delinsCCCAATAAGCCCCTGT XP_016876829.1:n.531-24_531-9delinsCCCAATAAGCCCCTGT
NM_000257.4:c.531-24_531-9delinsCCCAATAAGCCCCTGT MANE Select NP_000248.2:n.531-24_531-9delinsCCCAATAAGCCCCTGT
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