Canonical Allele Identifier: CA2123458994

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23413961_23413962delinsCT , CM000676.2:g.23413961_23413962delinsCT	GRCh38
NC_000014.8:g.23883170_23883171delinsCT , CM000676.1:g.23883170_23883171delinsCT	GRCh37
NC_000014.7:g.22953010_22953011delinsCT	NCBI36
NG_007884.1:g.26700_26701delinsAG , LRG_384:g.26700_26701delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.5655+45_5655+46delinsAG MANE Select	ENSP00000347507.3:n.5655+45_5655+46delinsAG
ENST00000355349.3:c.5655+45_5655+46delinsAG	ENSP00000347507.3:n.5655+45_5655+46delinsAG
NM_000257.3:c.5655+45_5655+46delinsAG	NP_000248.2:n.5655+45_5655+46delinsAG
XM_017021340.1:c.5655+45_5655+46delinsAG	XP_016876829.1:n.5655+45_5655+46delinsAG
NM_000257.4:c.5655+45_5655+46delinsAG MANE Select	NP_000248.2:n.5655+45_5655+46delinsAG