Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101554014_101554018delinsCTCTT , CM000672.2:g.101554014_101554018delinsCTCTT	GRCh38
NC_000010.10:g.103313771_103313775delinsCTCTT , CM000672.1:g.103313771_103313775delinsCTCTT	GRCh37
NC_000010.9:g.103303761_103303765delinsCTCTT	NCBI36
NG_009234.1:g.204947_204951delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370187.8:c.891_895delinsCTCTT MANE Select	ENSP00000359206.3:n.891_895delinsCTCTT
ENST00000370187.7:c.891_895delinsCTCTT	ENSP00000359206.3:n.891_895delinsCTCTT
ENST00000393441.8:c.891_895delinsCTCTT	ENSP00000377088.5:n.891_895delinsCTCTT
ENST00000408038.6:c.891_895delinsCTCTT	ENSP00000385339.2:n.891_895delinsCTCTT
NM_001256856.1:c.891_895delinsCTCTT	NP_001243785.1:n.891_895delinsCTCTT
NM_003939.4:c.891_895delinsCTCTT	NP_003930.1:n.891_895delinsCTCTT
NM_033637.3:c.891_895delinsCTCTT	NP_378663.1:n.891_895delinsCTCTT
XM_005270264.2:c.891_895delinsCTCTT	XP_005270321.1:n.891_895delinsCTCTT
XM_006718054.2:c.891_895delinsCTCTT	XP_006718117.1:n.891_895delinsCTCTT
XM_011540320.1:c.891_895delinsCTCTT	XP_011538622.1:n.891_895delinsCTCTT
XM_011540320.2:c.891_895delinsCTCTT	XP_011538622.1:n.891_895delinsCTCTT
XM_017016870.1:c.891_895delinsCTCTT	XP_016872359.1:n.891_895delinsCTCTT
XM_017016871.1:c.891_895delinsCTCTT	XP_016872360.1:n.891_895delinsCTCTT
XM_017016872.1:c.891_895delinsCTCTT	XP_016872361.1:n.891_895delinsCTCTT
XM_017016873.2:c.891_895delinsCTCTT	XP_016872362.1:n.891_895delinsCTCTT
XM_017016874.1:c.891_895delinsCTCTT	XP_016872363.1:n.891_895delinsCTCTT
XM_024448246.1:c.891_895delinsCTCTT	XP_024304014.1:n.891_895delinsCTCTT
XM_024448247.1:c.891_895delinsCTCTT	XP_024304015.1:n.891_895delinsCTCTT
XR_001747256.1:n.3060_3064delinsCTCTT
NM_033637.4:c.891_895delinsCTCTT MANE Select	NP_378663.1:n.891_895delinsCTCTT
NM_003939.5:c.891_895delinsCTCTT	NP_003930.1:n.891_895delinsCTCTT
NM_001256856.2:c.891_895delinsCTCTT	NP_001243785.1:n.891_895delinsCTCTT

HGVS	Amino-acid Change
ENST00000370187.8:c.891_895delinsCTCTT MANE Select	ENSP00000359206.3:n.891_895delinsCTCTT
ENST00000370187.7:c.891_895delinsCTCTT	ENSP00000359206.3:n.891_895delinsCTCTT
ENST00000393441.8:c.891_895delinsCTCTT	ENSP00000377088.5:n.891_895delinsCTCTT
ENST00000408038.6:c.891_895delinsCTCTT	ENSP00000385339.2:n.891_895delinsCTCTT
NM_001256856.1:c.891_895delinsCTCTT	NP_001243785.1:n.891_895delinsCTCTT
NM_003939.4:c.891_895delinsCTCTT	NP_003930.1:n.891_895delinsCTCTT
NM_033637.3:c.891_895delinsCTCTT	NP_378663.1:n.891_895delinsCTCTT
XM_005270264.2:c.891_895delinsCTCTT	XP_005270321.1:n.891_895delinsCTCTT
XM_006718054.2:c.891_895delinsCTCTT	XP_006718117.1:n.891_895delinsCTCTT
XM_011540320.1:c.891_895delinsCTCTT	XP_011538622.1:n.891_895delinsCTCTT
XM_011540320.2:c.891_895delinsCTCTT	XP_011538622.1:n.891_895delinsCTCTT
XM_017016870.1:c.891_895delinsCTCTT	XP_016872359.1:n.891_895delinsCTCTT
XM_017016871.1:c.891_895delinsCTCTT	XP_016872360.1:n.891_895delinsCTCTT
XM_017016872.1:c.891_895delinsCTCTT	XP_016872361.1:n.891_895delinsCTCTT
XM_017016873.2:c.891_895delinsCTCTT	XP_016872362.1:n.891_895delinsCTCTT
XM_017016874.1:c.891_895delinsCTCTT	XP_016872363.1:n.891_895delinsCTCTT
XM_024448246.1:c.891_895delinsCTCTT	XP_024304014.1:n.891_895delinsCTCTT
XM_024448247.1:c.891_895delinsCTCTT	XP_024304015.1:n.891_895delinsCTCTT
XR_001747256.1:n.3060_3064delinsCTCTT
NM_033637.4:c.891_895delinsCTCTT MANE Select	NP_378663.1:n.891_895delinsCTCTT
NM_003939.5:c.891_895delinsCTCTT	NP_003930.1:n.891_895delinsCTCTT
NM_001256856.2:c.891_895delinsCTCTT	NP_001243785.1:n.891_895delinsCTCTT