Canonical Allele Identifier: CA2123453900
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423924_23423925delinsGT , CM000676.2:g.23423924_23423925delinsGT GRCh38
NC_000014.8:g.23893133_23893134delinsGT , CM000676.1:g.23893133_23893134delinsGT GRCh37
NC_000014.7:g.22962973_22962974delinsGT NCBI36
NG_007884.1:g.16737_16738delinsAC , LRG_384:g.16737_16738delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2904_2905delinsAC MANE Select ENSP00000347507.3:p.Lys968=
ENST00000355349.3:c.2904_2905delinsAC ENSP00000347507.3:p.Lys968=
NM_000257.3:c.2904_2905delinsAC NP_000248.2:p.Lys968=
XR_245686.3:n.3010_3011delinsAC
XM_017021340.1:c.2904_2905delinsAC XP_016876829.1:p.Lys968=
NM_000257.4:c.2904_2905delinsAC MANE Select NP_000248.2:p.Lys968=