Canonical Allele Identifier: CA2123452912
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431865_23431866delinsCT , CM000676.2:g.23431865_23431866delinsCT GRCh38
NC_000014.8:g.23901074_23901075delinsCT , CM000676.1:g.23901074_23901075delinsCT GRCh37
NC_000014.7:g.22970914_22970915delinsCT NCBI36
NG_007884.1:g.8796_8797delinsAG , LRG_384:g.8796_8797delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.534_535delinsAG MANE Select ENSP00000347507.3:p.Gly178=
ENST00000355349.3:c.534_535delinsAG ENSP00000347507.3:p.Gly178=
NM_000257.3:c.534_535delinsAG NP_000248.2:p.Gly178=
XR_245686.3:n.640_641delinsAG
XM_017021340.1:c.534_535delinsAG XP_016876829.1:p.Gly178=
NM_000257.4:c.534_535delinsAG MANE Select NP_000248.2:p.Gly178=