Canonical Allele Identifier: CA2123450920
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431164_23431167delinsCAGA , CM000676.2:g.23431164_23431167delinsCAGA GRCh38
NC_000014.8:g.23900373_23900376delinsCAGA , CM000676.1:g.23900373_23900376delinsCAGA GRCh37
NC_000014.7:g.22970213_22970216delinsCAGA NCBI36
NG_007884.1:g.9495_9498delinsTCTG , LRG_384:g.9495_9498delinsTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-168_797-165delinsTCTG MANE Select ENSP00000347507.3:n.797-168_797-165delinsTCTG
ENST00000355349.3:c.797-168_797-165delinsTCTG ENSP00000347507.3:n.797-168_797-165delinsTCTG
NM_000257.3:c.797-168_797-165delinsTCTG NP_000248.2:n.797-168_797-165delinsTCTG
XR_245686.3:n.903-168_903-165delinsTCTG
XM_017021340.1:c.797-168_797-165delinsTCTG XP_016876829.1:n.797-168_797-165delinsTCTG
NM_000257.4:c.797-168_797-165delinsTCTG MANE Select NP_000248.2:n.797-168_797-165delinsTCTG