Canonical Allele Identifier: CA2123468913
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417420A= , CM000676.2:g.23417420A= GRCh38
NC_000014.8:g.23886629A= , CM000676.1:g.23886629A= GRCh37
NC_000014.7:g.22956469A= NCBI36
NG_007884.1:g.23242T= , LRG_384:g.23242T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4353+83T= (MYH7) MANE Select ENSP00000347507.3:n.4353+83T=
ENST00000355349.3:c.4353+83T= (MYH7) ENSP00000347507.3:n.4353+83T=
NM_000257.3:c.4353+83T= (MYH7) NP_000248.2:n.4353+83T=
NR_126491.1:n.813+47A= (MHRT)
XM_017021340.1:c.4353+83T= (MYH7) XP_016876829.1:n.4353+83T=
NM_000257.4:c.4353+83T= (MYH7) MANE Select NP_000248.2:n.4353+83T=
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