Canonical Allele Identifier: CA704289598
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1419658994
MyVariant Identifiers: chr14:g.23890487_23890488insA (hg19) chr14:g.23421278_23421279insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23421279dup , CM000676.2:g.23421279dup GRCh38
NC_000014.8:g.23890488dup , CM000676.1:g.23890488dup GRCh37
NC_000014.7:g.22960328dup NCBI36
NG_007884.1:g.19383dup , LRG_384:g.19383dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3246-231dup MANE Select ENSP00000347507.3:n.3246-231dup
ENST00000355349.3:c.3246-231dup ENSP00000347507.3:n.3246-231dup
NM_000257.3:c.3246-231dup NP_000248.2:n.3246-231dup
XR_245686.3:n.3354-231dup
XM_017021340.1:c.3246-231dup XP_016876829.1:n.3246-231dup
NM_000257.4:c.3246-231dup MANE Select NP_000248.2:n.3246-231dup
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