Canonical Allele Identifier: CA2123454010
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423958_23423959delinsCA , CM000676.2:g.23423958_23423959delinsCA GRCh38
NC_000014.8:g.23893167_23893168delinsCA , CM000676.1:g.23893167_23893168delinsCA GRCh37
NC_000014.7:g.22963007_22963008delinsCA NCBI36
NG_007884.1:g.16703_16704delinsTG , LRG_384:g.16703_16704delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2870_2871delinsTG MANE Select ENSP00000347507.3:p.Leu957=
ENST00000355349.3:c.2870_2871delinsTG ENSP00000347507.3:p.Leu957=
NM_000257.3:c.2870_2871delinsTG NP_000248.2:p.Leu957=
XR_245686.3:n.2976_2977delinsTG
XM_017021340.1:c.2870_2871delinsTG XP_016876829.1:p.Leu957=
NM_000257.4:c.2870_2871delinsTG MANE Select NP_000248.2:p.Leu957=