Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34880615_34880623delinsGGCTGCGGT , CM000683.2:g.34880615_34880623delinsGGCTGCGGT	GRCh38
NC_000021.8:g.36252912_36252920delinsGGCTGCGGT , CM000683.1:g.36252912_36252920delinsGGCTGCGGT	GRCh37
NC_000021.7:g.35174782_35174790delinsGGCTGCGGT	NCBI36
NG_011402.2:g.1109089_1109097delinsACCGCAGCC , LRG_482:g.1109089_1109097delinsACCGCAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675419.1:c.442_450delinsACCGCAGCC MANE Select	ENSP00000501943.1:p.Thr148=
ENST00000300305.7:c.442_450delinsACCGCAGCC	ENSP00000300305.3:p.Thr148=
ENST00000344691.8:c.361_369delinsACCGCAGCC	ENSP00000340690.4:p.Thr121=
ENST00000358356.9:c.361_369delinsACCGCAGCC	ENSP00000351123.5:p.Thr121=
ENST00000399237.6:c.406_414delinsACCGCAGCC	ENSP00000382182.2:p.Thr136=
ENST00000399240.5:c.361_369delinsACCGCAGCC	ENSP00000382184.1:p.Thr121=
ENST00000437180.5:c.442_450delinsACCGCAGCC	ENSP00000409227.1:p.Thr148=
ENST00000455571.5:c.403_411delinsACCGCAGCC	ENSP00000388189.1:p.Thr135=
ENST00000482318.5:c.32_40delinsACCGCAGCC	ENSP00000477067.1:n.32_40delinsACCGCAGCC
NM_001001890.2:c.361_369delinsACCGCAGCC	NP_001001890.1:p.Thr121=
NM_001122607.1:c.361_369delinsACCGCAGCC	NP_001116079.1:p.Thr121=
NM_001754.4:c.442_450delinsACCGCAGCC , LRG_482t1:c.442_450delinsACCGCAGCC	NP_001745.2:p.Thr148=
XM_005261068.3:c.406_414delinsACCGCAGCC	XP_005261125.1:p.Thr136=
XM_005261069.3:c.442_450delinsACCGCAGCC	XP_005261126.1:p.Thr148=
XM_011529766.1:c.442_450delinsACCGCAGCC	XP_011528068.1:p.Thr148=
XM_011529767.1:c.403_411delinsACCGCAGCC	XP_011528069.1:p.Thr135=
XM_011529768.1:c.403_411delinsACCGCAGCC	XP_011528070.1:p.Thr135=
XM_011529770.1:c.442_450delinsACCGCAGCC	XP_011528072.1:p.Thr148=
XR_937576.1:n.621_629delinsACCGCAGCC
XM_005261069.4:c.442_450delinsACCGCAGCC	XP_005261126.1:p.Thr148=
XM_011529766.2:c.442_450delinsACCGCAGCC	XP_011528068.1:p.Thr148=
XM_011529767.2:c.403_411delinsACCGCAGCC	XP_011528069.1:p.Thr135=
XM_011529768.2:c.403_411delinsACCGCAGCC	XP_011528070.1:p.Thr135=
XM_011529770.2:c.442_450delinsACCGCAGCC	XP_011528072.1:p.Thr148=
XM_017028487.1:c.289_297delinsACCGCAGCC	XP_016883976.1:p.Thr97=
XR_937576.2:n.668_676delinsACCGCAGCC
NM_001001890.3:c.361_369delinsACCGCAGCC	NP_001001890.1:p.Thr121=
NM_001122607.2:c.361_369delinsACCGCAGCC	NP_001116079.1:p.Thr121=
NM_001754.5:c.442_450delinsACCGCAGCC MANE Select	NP_001745.2:p.Thr148=