Canonical Allele Identifier: CA2123452773
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431831_23431832delinsCT , CM000676.2:g.23431831_23431832delinsCT GRCh38
NC_000014.8:g.23901040_23901041delinsCT , CM000676.1:g.23901040_23901041delinsCT GRCh37
NC_000014.7:g.22970880_22970881delinsCT NCBI36
NG_007884.1:g.8830_8831delinsAG , LRG_384:g.8830_8831delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.568_569delinsAG MANE Select ENSP00000347507.3:p.Arg190=
ENST00000355349.3:c.568_569delinsAG ENSP00000347507.3:p.Arg190=
NM_000257.3:c.568_569delinsAG NP_000248.2:p.Arg190=
XR_245686.3:n.674_675delinsAG
XM_017021340.1:c.568_569delinsAG XP_016876829.1:p.Arg190=
NM_000257.4:c.568_569delinsAG MANE Select NP_000248.2:p.Arg190=