Allele Registry

HGVS	Genome Assembly
NC_000014.9:g.23415905_23415910delinsTCCCTG , CM000676.2:g.23415905_23415910delinsTCCCTG	GRCh38
NC_000014.8:g.23885114_23885119delinsTCCCTG , CM000676.1:g.23885114_23885119delinsTCCCTG	GRCh37
NC_000014.7:g.22954954_22954959delinsTCCCTG	NCBI36
NG_007884.1:g.24752_24757delinsCAGGGA , LRG_384:g.24752_24757delinsCAGGGA

HGVS	Amino-acid Change
ENST00000355349.4:c.4954-78_4954-73delinsCAGGGA (MYH7) MANE Select	ENSP00000347507.3:n.4954-78_4954-73delinsCAGGGA
ENST00000355349.3:c.4954-78_4954-73delinsCAGGGA (MYH7)	ENSP00000347507.3:n.4954-78_4954-73delinsCAGGGA
NM_000257.3:c.4954-78_4954-73delinsCAGGGA (MYH7)	NP_000248.2:n.4954-78_4954-73delinsCAGGGA
NR_126491.1:n.261+76_261+81delinsTCCCTG (MHRT)
XM_017021340.1:c.4954-78_4954-73delinsCAGGGA (MYH7)	XP_016876829.1:n.4954-78_4954-73delinsCAGGGA
NM_000257.4:c.4954-78_4954-73delinsCAGGGA (MYH7) MANE Select	NP_000248.2:n.4954-78_4954-73delinsCAGGGA