Canonical Allele Identifier: CA2123465326
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416104_23416107delinsATCT , CM000676.2:g.23416104_23416107delinsATCT GRCh38
NC_000014.8:g.23885313_23885316delinsATCT , CM000676.1:g.23885313_23885316delinsATCT GRCh37
NC_000014.7:g.22955153_22955156delinsATCT NCBI36
NG_007884.1:g.24555_24558delinsAGAT , LRG_384:g.24555_24558delinsAGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4850_4853delinsAGAT (MYH7) MANE Select ENSP00000347507.3:p.Lys1617=
ENST00000355349.3:c.4850_4853delinsAGAT (MYH7) ENSP00000347507.3:p.Lys1617=
NM_000257.3:c.4850_4853delinsAGAT (MYH7) NP_000248.2:p.Lys1617=
NR_126491.1:n.365_368delinsATCT (MHRT)
XM_017021340.1:c.4850_4853delinsAGAT (MYH7) XP_016876829.1:p.Lys1617=
NM_000257.4:c.4850_4853delinsAGAT (MYH7) MANE Select NP_000248.2:p.Lys1617=
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