Canonical Allele Identifier: CA2123453624
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423756_23423757delinsCA , CM000676.2:g.23423756_23423757delinsCA GRCh38
NC_000014.8:g.23892965_23892966delinsCA , CM000676.1:g.23892965_23892966delinsCA GRCh37
NC_000014.7:g.22962805_22962806delinsCA NCBI36
NG_007884.1:g.16905_16906delinsTG , LRG_384:g.16905_16906delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2923-34_2923-33delinsTG MANE Select ENSP00000347507.3:n.2923-34_2923-33delinsTG
ENST00000355349.3:c.2923-34_2923-33delinsTG ENSP00000347507.3:n.2923-34_2923-33delinsTG
NM_000257.3:c.2923-34_2923-33delinsTG NP_000248.2:n.2923-34_2923-33delinsTG
XR_245686.3:n.3029-34_3029-33delinsTG
XM_017021340.1:c.2923-34_2923-33delinsTG XP_016876829.1:n.2923-34_2923-33delinsTG
NM_000257.4:c.2923-34_2923-33delinsTG MANE Select NP_000248.2:n.2923-34_2923-33delinsTG