Canonical Allele Identifier: CA2586967111

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99916483_99916485dup , CM000663.2:g.99916483_99916485dup	GRCh38
NC_000001.10:g.100382039_100382041dup , CM000663.1:g.100382039_100382041dup	GRCh37
NC_000001.9:g.100154627_100154629dup	NCBI36
NG_012865.1:g.71400_71402dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4333_4335dup MANE Select	ENSP00000355106.3:p.Tyr1445_His1446insTyr
ENST00000637337.1:n.4544_4546dup
ENST00000294724.8:c.4333_4335dup	ENSP00000294724.4:p.Tyr1445_His1446insTyr
ENST00000361302.7:c.4285_4287dup	ENSP00000354971.3:p.Tyr1429_His1430insTyr
ENST00000361522.4:c.4282_4284dup	ENSP00000354635.4:p.Tyr1428_His1429insTyr
ENST00000361915.7:c.4333_4335dup	ENSP00000355106.3:p.Tyr1445_His1446insTyr
ENST00000370161.6:c.4285_4287dup	ENSP00000359180.2:p.Tyr1429_His1430insTyr
ENST00000370163.7:c.4333_4335dup	ENSP00000359182.3:p.Tyr1445_His1446insTyr
ENST00000370165.7:c.4333_4335dup	ENSP00000359184.3:p.Tyr1445_His1446insTyr
NM_000028.2:c.4333_4335dup	NP_000019.2:p.Tyr1445_His1446insTyr
NM_000642.2:c.4333_4335dup	NP_000633.2:p.Tyr1445_His1446insTyr
NM_000643.2:c.4333_4335dup	NP_000634.2:p.Tyr1445_His1446insTyr
NM_000644.2:c.4333_4335dup	NP_000635.2:p.Tyr1445_His1446insTyr
NM_000645.2:c.4282_4284dup	NP_000636.2:p.Tyr1428_His1429insTyr
NM_000646.2:c.4285_4287dup	NP_000637.2:p.Tyr1429_His1430insTyr
XM_005270557.1:c.4333_4335dup	XP_005270614.1:p.Tyr1445_His1446insTyr
XR_947626.1:n.1318-3266_1318-3264dup
XR_947627.1:n.1207-3266_1207-3264dup
XR_947628.1:n.1312-3266_1312-3264dup
XR_947630.1:n.1250-3266_1250-3264dup
XR_947632.1:n.1136-3266_1136-3264dup
XR_947633.1:n.1247-3266_1247-3264dup
XR_947634.1:n.661-3266_661-3264dup
XR_947635.1:n.729-3266_729-3264dup
XM_005270557.2:c.4333_4335dup	XP_005270614.1:p.Tyr1445_His1446insTyr
XM_017000501.2:c.2593_2595dup	XP_016855990.1:p.Tyr865_His866insTyr
NM_000642.3:c.4333_4335dup MANE Select	NP_000633.2:p.Tyr1445_His1446insTyr