Canonical Allele Identifier: CA1183944919

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921600_99921602delinsAAC , CM000663.2:g.99921600_99921602delinsAAC	GRCh38
NC_000001.10:g.100387156_100387158delinsAAC , CM000663.1:g.100387156_100387158delinsAAC	GRCh37
NC_000001.9:g.100159744_100159746delinsAAC	NCBI36
NG_012865.1:g.76517_76519delinsAAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.4548_4550delinsAAC MANE Select	ENSP00000355106.3:p.Glu1516=
ENST00000637337.1:n.4759_4761delinsAAC
ENST00000294724.8:c.4548_4550delinsAAC	ENSP00000294724.4:p.Glu1516=
ENST00000361302.7:c.4500_4502delinsAAC	ENSP00000354971.3:p.Glu1500=
ENST00000361522.4:c.4497_4499delinsAAC	ENSP00000354635.4:p.Glu1499=
ENST00000361915.7:c.4548_4550delinsAAC	ENSP00000355106.3:p.Glu1516=
ENST00000370161.6:c.4500_4502delinsAAC	ENSP00000359180.2:p.Glu1500=
ENST00000370163.7:c.4548_4550delinsAAC	ENSP00000359182.3:p.Glu1516=
ENST00000370165.7:c.4548_4550delinsAAC	ENSP00000359184.3:p.Glu1516=
NM_000028.2:c.4548_4550delinsAAC	NP_000019.2:p.Glu1516=
NM_000642.2:c.4548_4550delinsAAC	NP_000633.2:p.Glu1516=
NM_000643.2:c.4548_4550delinsAAC	NP_000634.2:p.Glu1516=
NM_000644.2:c.4548_4550delinsAAC	NP_000635.2:p.Glu1516=
NM_000645.2:c.4497_4499delinsAAC	NP_000636.2:p.Glu1499=
NM_000646.2:c.4500_4502delinsAAC	NP_000637.2:p.Glu1500=
XM_005270557.1:c.4548_4550delinsAAC	XP_005270614.1:p.Glu1516=
XR_947626.1:n.1317+2636_1317+2638delinsGTT
XR_947627.1:n.1206+2636_1206+2638delinsGTT
XR_947628.1:n.1311+2636_1311+2638delinsGTT
XR_947630.1:n.1249+2636_1249+2638delinsGTT
XR_947632.1:n.1135+2636_1135+2638delinsGTT
XR_947633.1:n.1246+2636_1246+2638delinsGTT
XR_947634.1:n.660+2636_660+2638delinsGTT
XR_947635.1:n.728+2636_728+2638delinsGTT
XM_005270557.2:c.4548_4550delinsAAC	XP_005270614.1:p.Glu1516=
XM_017000501.2:c.2808_2810delinsAAC	XP_016855990.1:p.Glu936=
NM_000642.3:c.4548_4550delinsAAC MANE Select	NP_000633.2:p.Glu1516=