Canonical Allele Identifier: CA704291104
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1435194704

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423428_23423437del , CM000676.2:g.23423428_23423437del GRCh38
NC_000014.8:g.23892637_23892646del , CM000676.1:g.23892637_23892646del GRCh37
NC_000014.7:g.22962477_22962486del NCBI36
NG_007884.1:g.17226_17235del , LRG_384:g.17226_17235del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+111_3099+120del MANE Select ENSP00000347507.3:n.3099+111_3099+120del
ENST00000355349.3:c.3099+111_3099+120del ENSP00000347507.3:n.3099+111_3099+120del
NM_000257.3:c.3099+111_3099+120del NP_000248.2:n.3099+111_3099+120del
XR_245686.3:n.3205+111_3205+120del
XM_017021340.1:c.3099+111_3099+120del XP_016876829.1:n.3099+111_3099+120del
NM_000257.4:c.3099+111_3099+120del MANE Select NP_000248.2:n.3099+111_3099+120del