Canonical Allele Identifier: CA2123445772

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419719_23419726delinsGGGGATCT , CM000676.2:g.23419719_23419726delinsGGGGATCT	GRCh38
NC_000014.8:g.23888928_23888935delinsGGGGATCT , CM000676.1:g.23888928_23888935delinsGGGGATCT	GRCh37
NC_000014.7:g.22958768_22958775delinsGGGGATCT	NCBI36
NG_007884.1:g.20936_20943delinsAGATCCCC , LRG_384:g.20936_20943delinsAGATCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3727-117_3727-110delinsAGATCCCC MANE Select	ENSP00000347507.3:n.3727-117_3727-110delinsAGATCCCC
ENST00000355349.3:c.3727-117_3727-110delinsAGATCCCC	ENSP00000347507.3:n.3727-117_3727-110delinsAGATCCCC
NM_000257.3:c.3727-117_3727-110delinsAGATCCCC	NP_000248.2:n.3727-117_3727-110delinsAGATCCCC
XM_017021340.1:c.3727-117_3727-110delinsAGATCCCC	XP_016876829.1:n.3727-117_3727-110delinsAGATCCCC
NM_000257.4:c.3727-117_3727-110delinsAGATCCCC MANE Select	NP_000248.2:n.3727-117_3727-110delinsAGATCCCC