Canonical Allele Identifier: CA389046463
Community Standard Title: NM_000257.4(MYH7):c.2945T>A (p.Met982Lys)
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423701A>T , CM000676.2:g.23423701A>T GRCh38
NC_000014.8:g.23892910A>T , CM000676.1:g.23892910A>T GRCh37
NC_000014.7:g.22962750A>T NCBI36
NG_007884.1:g.16961T>A , LRG_384:g.16961T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.2945T>A MANE Select NP_000248.2:p.Met982Lys
ENST00000355349.4:c.2945T>A MANE Select ENSP00000347507.3:p.Met982Lys
NM_000257.3:c.2945T>A NP_000248.2:p.Met982Lys
ENST00000355349.3:c.2945T>A ENSP00000347507.3:p.Met982Lys
XM_017021340.1:c.2945T>A XP_016876829.1:p.Met982Lys
XR_245686.3:n.3051T>A
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