Canonical Allele Identifier: CA2123448355

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420851_23420853delinsCAT , CM000676.2:g.23420851_23420853delinsCAT	GRCh38
NC_000014.8:g.23890060_23890062delinsCAT , CM000676.1:g.23890060_23890062delinsCAT	GRCh37
NC_000014.7:g.22959900_22959902delinsCAT	NCBI36
NG_007884.1:g.19809_19811delinsATG , LRG_384:g.19809_19811delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3336+105_3336+107delinsATG MANE Select	ENSP00000347507.3:n.3336+105_3336+107delinsATG
ENST00000355349.3:c.3336+105_3336+107delinsATG	ENSP00000347507.3:n.3336+105_3336+107delinsATG
NM_000257.3:c.3336+105_3336+107delinsATG	NP_000248.2:n.3336+105_3336+107delinsATG
XR_245686.3:n.3444+105_3444+107delinsATG
XM_017021340.1:c.3336+105_3336+107delinsATG	XP_016876829.1:n.3336+105_3336+107delinsATG
NM_000257.4:c.3336+105_3336+107delinsATG MANE Select	NP_000248.2:n.3336+105_3336+107delinsATG