Canonical Allele Identifier: CA2624233447
Gene: MYH7 HGNC NCBI

Linked Data

gnomAD v4: 14-23421135-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23421136dup , CM000676.2:g.23421136dup GRCh38
NC_000014.8:g.23890345dup , CM000676.1:g.23890345dup GRCh37
NC_000014.7:g.22960185dup NCBI36
NG_007884.1:g.19526dup , LRG_384:g.19526dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3246-88dup MANE Select ENSP00000347507.3:n.3246-88dup
ENST00000355349.3:c.3246-88dup ENSP00000347507.3:n.3246-88dup
NM_000257.3:c.3246-88dup NP_000248.2:n.3246-88dup
XR_245686.3:n.3354-88dup
XM_017021340.1:c.3246-88dup XP_016876829.1:n.3246-88dup
NM_000257.4:c.3246-88dup MANE Select NP_000248.2:n.3246-88dup
Search 100 bp 5'
Search 100 bp 3'