Canonical Allele Identifier: CA2123451138
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431324_23431328delinsCAGAG , CM000676.2:g.23431324_23431328delinsCAGAG GRCh38
NC_000014.8:g.23900533_23900537delinsCAGAG , CM000676.1:g.23900533_23900537delinsCAGAG GRCh37
NC_000014.7:g.22970373_22970377delinsCAGAG NCBI36
NG_007884.1:g.9334_9338delinsCTCTG , LRG_384:g.9334_9338delinsCTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.796+90_796+94delinsCTCTG MANE Select ENSP00000347507.3:n.796+90_796+94delinsCTCTG
ENST00000355349.3:c.796+90_796+94delinsCTCTG ENSP00000347507.3:n.796+90_796+94delinsCTCTG
NM_000257.3:c.796+90_796+94delinsCTCTG NP_000248.2:n.796+90_796+94delinsCTCTG
XR_245686.3:n.902+90_902+94delinsCTCTG
XM_017021340.1:c.796+90_796+94delinsCTCTG XP_016876829.1:n.796+90_796+94delinsCTCTG
NM_000257.4:c.796+90_796+94delinsCTCTG MANE Select NP_000248.2:n.796+90_796+94delinsCTCTG