Canonical Allele Identifier: CA2800863399

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423438_23423439insCC , CM000676.2:g.23423438_23423439insCC	GRCh38
NC_000014.8:g.23892647_23892648insCC , CM000676.1:g.23892647_23892648insCC	GRCh37
NC_000014.7:g.22962487_22962488insCC	NCBI36
NG_007884.1:g.17224_17225insGG , LRG_384:g.17224_17225insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+109_3099+110insGG MANE Select	ENSP00000347507.3:n.3099+109_3099+110insGG
ENST00000355349.3:c.3099+109_3099+110insGG	ENSP00000347507.3:n.3099+109_3099+110insGG
NM_000257.3:c.3099+109_3099+110insGG	NP_000248.2:n.3099+109_3099+110insGG
XR_245686.3:n.3205+109_3205+110insGG
XM_017021340.1:c.3099+109_3099+110insGG	XP_016876829.1:n.3099+109_3099+110insGG
NM_000257.4:c.3099+109_3099+110insGG MANE Select	NP_000248.2:n.3099+109_3099+110insGG