Canonical Allele Identifier: CA2123466361

Gene: MYH7 MHRT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23416351_23416353delinsCAG , CM000676.2:g.23416351_23416353delinsCAG	GRCh38
NC_000014.8:g.23885560_23885562delinsCAG , CM000676.1:g.23885560_23885562delinsCAG	GRCh37
NC_000014.7:g.22955400_22955402delinsCAG	NCBI36
NG_007884.1:g.24309_24311delinsCTG , LRG_384:g.24309_24311delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4645-41_4645-39delinsCTG (MYH7) MANE Select	ENSP00000347507.3:n.4645-41_4645-39delinsCTG
ENST00000355349.3:c.4645-41_4645-39delinsCTG (MYH7)	ENSP00000347507.3:n.4645-41_4645-39delinsCTG
NM_000257.3:c.4645-41_4645-39delinsCTG (MYH7)	NP_000248.2:n.4645-41_4645-39delinsCTG
NR_126491.1:n.558+54_558+56delinsCAG (MHRT)
XM_017021340.1:c.4645-41_4645-39delinsCTG (MYH7)	XP_016876829.1:n.4645-41_4645-39delinsCTG
NM_000257.4:c.4645-41_4645-39delinsCTG (MYH7) MANE Select	NP_000248.2:n.4645-41_4645-39delinsCTG