Canonical Allele Identifier: CA2533355979
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429192_23429193del , CM000676.2:g.23429192_23429193del GRCh38
NC_000014.8:g.23898401_23898402del , CM000676.1:g.23898401_23898402del GRCh37
NC_000014.7:g.22968241_22968242del NCBI36
NG_007884.1:g.11469_11470del , LRG_384:g.11469_11470del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1257+36_1257+37del MANE Select ENSP00000347507.3:n.1257+36_1257+37del
ENST00000355349.3:c.1257+36_1257+37del ENSP00000347507.3:n.1257+36_1257+37del
NM_000257.3:c.1257+36_1257+37del NP_000248.2:n.1257+36_1257+37del
XR_245686.3:n.1363+36_1363+37del
XM_017021340.1:c.1257+36_1257+37del XP_016876829.1:n.1257+36_1257+37del
NM_000257.4:c.1257+36_1257+37del MANE Select NP_000248.2:n.1257+36_1257+37del