Canonical Allele Identifier: CA2573050136
Gene: MYH7 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423436_23423440delinsAACAC , CM000676.2:g.23423436_23423440delinsAACAC GRCh38
NC_000014.8:g.23892645_23892649delinsAACAC , CM000676.1:g.23892645_23892649delinsAACAC GRCh37
NC_000014.7:g.22962485_22962489delinsAACAC NCBI36
NG_007884.1:g.17222_17226delinsGTGTT , LRG_384:g.17222_17226delinsGTGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+107_3099+111delinsGTGTT MANE Select ENSP00000347507.3:n.3099+107_3099+111delinsGTGTT
ENST00000355349.3:c.3099+107_3099+111delinsGTGTT ENSP00000347507.3:n.3099+107_3099+111delinsGTGTT
NM_000257.3:c.3099+107_3099+111delinsGTGTT NP_000248.2:n.3099+107_3099+111delinsGTGTT
XR_245686.3:n.3205+107_3205+111delinsGTGTT
XM_017021340.1:c.3099+107_3099+111delinsGTGTT XP_016876829.1:n.3099+107_3099+111delinsGTGTT
NM_000257.4:c.3099+107_3099+111delinsGTGTT MANE Select NP_000248.2:n.3099+107_3099+111delinsGTGTT
Search 100 bp 5'
Search 100 bp 3'