Allele Registry

HGVS	Genome Assembly
NC_000014.9:g.23423478_23423488delinsCACACACACAG , CM000676.2:g.23423478_23423488delinsCACACACACAG	GRCh38
NC_000014.8:g.23892687_23892697delinsCACACACACAG , CM000676.1:g.23892687_23892697delinsCACACACACAG	GRCh37
NC_000014.7:g.22962527_22962537delinsCACACACACAG	NCBI36
NG_007884.1:g.17174_17184delinsCTGTGTGTGTG , LRG_384:g.17174_17184delinsCTGTGTGTGTG

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+59_3099+69delinsCTGTGTGTGTG MANE Select	ENSP00000347507.3:n.3099+59_3099+69delinsCTGTGTGTGTG
ENST00000355349.3:c.3099+59_3099+69delinsCTGTGTGTGTG	ENSP00000347507.3:n.3099+59_3099+69delinsCTGTGTGTGTG
NM_000257.3:c.3099+59_3099+69delinsCTGTGTGTGTG	NP_000248.2:n.3099+59_3099+69delinsCTGTGTGTGTG
XR_245686.3:n.3205+59_3205+69delinsCTGTGTGTGTG
XM_017021340.1:c.3099+59_3099+69delinsCTGTGTGTGTG	XP_016876829.1:n.3099+59_3099+69delinsCTGTGTGTGTG
NM_000257.4:c.3099+59_3099+69delinsCTGTGTGTGTG MANE Select	NP_000248.2:n.3099+59_3099+69delinsCTGTGTGTGTG