Canonical Allele Identifier: CA2624238926
Gene: MYH7 HGNC NCBI

Linked Data

gnomAD v4: 14-23417800-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417801del , CM000676.2:g.23417801del GRCh38
NC_000014.8:g.23887010del , CM000676.1:g.23887010del GRCh37
NC_000014.7:g.22956850del NCBI36
NG_007884.1:g.22861del , LRG_384:g.22861del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4170-115del MANE Select ENSP00000347507.3:n.4170-115del
ENST00000355349.3:c.4170-115del ENSP00000347507.3:n.4170-115del
NM_000257.3:c.4170-115del NP_000248.2:n.4170-115del
XM_017021340.1:c.4170-115del XP_016876829.1:n.4170-115del
NM_000257.4:c.4170-115del MANE Select NP_000248.2:n.4170-115del
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