Allele Registry

HGVS	Genome Assembly
NC_000010.11:g.8064140delinsGCTTACTTCCC , CM000672.2:g.8064140delinsGCTTACTTCCC	GRCh38
NC_000010.10:g.8106103delinsGCTTACTTCCC , CM000672.1:g.8106103delinsGCTTACTTCCC	GRCh37
NC_000010.9:g.8146109delinsGCTTACTTCCC	NCBI36
NG_015859.1:g.14437delinsGCTTACTTCCC

HGVS	Amino-acid Change
ENST00000346208.4:c.921+2delinsGCTTACTTCCC	ENSP00000341619.3:n.921+2delinsGCTTACTTCCC
ENST00000379328.9:c.924+2delinsGCTTACTTCCC MANE Select	ENSP00000368632.3:n.924+2delinsGCTTACTTCCC
ENST00000346208.3:c.921+2delinsGCTTACTTCCC	ENSP00000341619.3:n.921+2delinsGCTTACTTCCC
ENST00000379328.7:c.924+2delinsGCTTACTTCCC	ENSP00000368632.3:n.924+2delinsGCTTACTTCCC
ENST00000461472.1:n.443+5299delinsGCTTACTTCCC
NM_001002295.1:c.924+2delinsGCTTACTTCCC	NP_001002295.1:n.924+2delinsGCTTACTTCCC
NM_002051.2:c.921+2delinsGCTTACTTCCC	NP_002042.1:n.921+2delinsGCTTACTTCCC
XM_005252442.2:c.924+2delinsGCTTACTTCCC	XP_005252499.1:n.924+2delinsGCTTACTTCCC
XM_005252443.3:c.924+2delinsGCTTACTTCCC	XP_005252500.1:n.924+2delinsGCTTACTTCCC
XM_005252443.5:c.924+2delinsGCTTACTTCCC	XP_005252500.1:n.924+2delinsGCTTACTTCCC
NM_001002295.2:c.924+2delinsGCTTACTTCCC MANE Select	NP_001002295.1:n.924+2delinsGCTTACTTCCC
NM_002051.3:c.921+2delinsGCTTACTTCCC	NP_002042.1:n.921+2delinsGCTTACTTCCC