Canonical Allele Identifier: CA2123454233
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424035_23424038delinsTCTC , CM000676.2:g.23424035_23424038delinsTCTC GRCh38
NC_000014.8:g.23893244_23893247delinsTCTC , CM000676.1:g.23893244_23893247delinsTCTC GRCh37
NC_000014.7:g.22963084_22963087delinsTCTC NCBI36
NG_007884.1:g.16624_16627delinsGAGA , LRG_384:g.16624_16627delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2791_2794delinsGAGA MANE Select ENSP00000347507.3:p.Glu931=
ENST00000355349.3:c.2791_2794delinsGAGA ENSP00000347507.3:p.Glu931=
NM_000257.3:c.2791_2794delinsGAGA NP_000248.2:p.Glu931=
XR_245686.3:n.2897_2900delinsGAGA
XM_017021340.1:c.2791_2794delinsGAGA XP_016876829.1:p.Glu931=
NM_000257.4:c.2791_2794delinsGAGA MANE Select NP_000248.2:p.Glu931=