Canonical Allele Identifier: CA2800863414

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423441_23423442insAATAA , CM000676.2:g.23423441_23423442insAATAA	GRCh38
NC_000014.8:g.23892650_23892651insAATAA , CM000676.1:g.23892650_23892651insAATAA	GRCh37
NC_000014.7:g.22962490_22962491insAATAA	NCBI36
NG_007884.1:g.17221_17222insTATTT , LRG_384:g.17221_17222insTATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+106_3099+107insTATTT MANE Select	ENSP00000347507.3:n.3099+106_3099+107insTATTT
ENST00000355349.3:c.3099+106_3099+107insTATTT	ENSP00000347507.3:n.3099+106_3099+107insTATTT
NM_000257.3:c.3099+106_3099+107insTATTT	NP_000248.2:n.3099+106_3099+107insTATTT
XR_245686.3:n.3205+106_3205+107insTATTT
XM_017021340.1:c.3099+106_3099+107insTATTT	XP_016876829.1:n.3099+106_3099+107insTATTT
NM_000257.4:c.3099+106_3099+107insTATTT MANE Select	NP_000248.2:n.3099+106_3099+107insTATTT