Canonical Allele Identifier: CA2123451139
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431324_23431326delinsCAG , CM000676.2:g.23431324_23431326delinsCAG GRCh38
NC_000014.8:g.23900533_23900535delinsCAG , CM000676.1:g.23900533_23900535delinsCAG GRCh37
NC_000014.7:g.22970373_22970375delinsCAG NCBI36
NG_007884.1:g.9336_9338delinsCTG , LRG_384:g.9336_9338delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.796+92_796+94delinsCTG MANE Select ENSP00000347507.3:n.796+92_796+94delinsCTG
ENST00000355349.3:c.796+92_796+94delinsCTG ENSP00000347507.3:n.796+92_796+94delinsCTG
NM_000257.3:c.796+92_796+94delinsCTG NP_000248.2:n.796+92_796+94delinsCTG
XR_245686.3:n.902+92_902+94delinsCTG
XM_017021340.1:c.796+92_796+94delinsCTG XP_016876829.1:n.796+92_796+94delinsCTG
NM_000257.4:c.796+92_796+94delinsCTG MANE Select NP_000248.2:n.796+92_796+94delinsCTG