Canonical Allele Identifier: CA2123452643
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423413_23423414delinsAC , CM000676.2:g.23423413_23423414delinsAC GRCh38
NC_000014.8:g.23892622_23892623delinsAC , CM000676.1:g.23892622_23892623delinsAC GRCh37
NC_000014.7:g.22962462_22962463delinsAC NCBI36
NG_007884.1:g.17248_17249delinsGT , LRG_384:g.17248_17249delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+133_3099+134delinsGT MANE Select ENSP00000347507.3:n.3099+133_3099+134delinsGT
ENST00000355349.3:c.3099+133_3099+134delinsGT ENSP00000347507.3:n.3099+133_3099+134delinsGT
NM_000257.3:c.3099+133_3099+134delinsGT NP_000248.2:n.3099+133_3099+134delinsGT
XR_245686.3:n.3205+133_3205+134delinsGT
XM_017021340.1:c.3099+133_3099+134delinsGT XP_016876829.1:n.3099+133_3099+134delinsGT
NM_000257.4:c.3099+133_3099+134delinsGT MANE Select NP_000248.2:n.3099+133_3099+134delinsGT