Canonical Allele Identifier: CA2624238987
Gene: MYH7 HGNC NCBI

Linked Data

gnomAD v4: 14-23417821-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417822del , CM000676.2:g.23417822del GRCh38
NC_000014.8:g.23887031del , CM000676.1:g.23887031del GRCh37
NC_000014.7:g.22956871del NCBI36
NG_007884.1:g.22840del , LRG_384:g.22840del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4170-136del MANE Select ENSP00000347507.3:n.4170-136del
ENST00000355349.3:c.4170-136del ENSP00000347507.3:n.4170-136del
NM_000257.3:c.4170-136del NP_000248.2:n.4170-136del
XM_017021340.1:c.4170-136del XP_016876829.1:n.4170-136del
NM_000257.4:c.4170-136del MANE Select NP_000248.2:n.4170-136del
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