Canonical Allele Identifier: CA2123452815
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431843_23431847delinsACTGT , CM000676.2:g.23431843_23431847delinsACTGT GRCh38
NC_000014.8:g.23901052_23901056delinsACTGT , CM000676.1:g.23901052_23901056delinsACTGT GRCh37
NC_000014.7:g.22970892_22970896delinsACTGT NCBI36
NG_007884.1:g.8815_8819delinsACAGT , LRG_384:g.8815_8819delinsACAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.553_557delinsACAGT MANE Select ENSP00000347507.3:p.Thr185=
ENST00000355349.3:c.553_557delinsACAGT ENSP00000347507.3:p.Thr185=
NM_000257.3:c.553_557delinsACAGT NP_000248.2:p.Thr185=
XR_245686.3:n.659_663delinsACAGT
XM_017021340.1:c.553_557delinsACAGT XP_016876829.1:p.Thr185=
NM_000257.4:c.553_557delinsACAGT MANE Select NP_000248.2:p.Thr185=