Canonical Allele Identifier: CA1183945117

Gene: AGL

Linked Data

• dbSNP Id: rs1655529980

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921799_99921800insCACAACTAAAAGAAC , CM000663.2:g.99921799_99921800insCACAACTAAAAGAAC	GRCh38
NC_000001.10:g.100387355_100387356insCACAACTAAAAGAAC , CM000663.1:g.100387355_100387356insCACAACTAAAAGAAC	GRCh37
NC_000001.9:g.100159943_100159944insCACAACTAAAAGAAC	NCBI36
NG_012865.1:g.76716_76717insCACAACTAAAAGAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.*148_*149insCACAACTAAAAGAAC MANE Select	ENSP00000355106.3:n.*148_*149insCACAACTAAAAGAAC
ENST00000637337.1:n.4958_4959insCACAACTAAAAGAAC
ENST00000294724.8:c.*148_*149insCACAACTAAAAGAAC	ENSP00000294724.4:n.*148_*149insCACAACTAAAAGAAC
ENST00000361302.7:c.*148_*149insCACAACTAAAAGAAC	ENSP00000354971.3:n.*148_*149insCACAACTAAAAGAAC
ENST00000361522.4:c.*148_*149insCACAACTAAAAGAAC	ENSP00000354635.4:n.*148_*149insCACAACTAAAAGAAC
ENST00000361915.7:c.*148_*149insCACAACTAAAAGAAC	ENSP00000355106.3:n.*148_*149insCACAACTAAAAGAAC
ENST00000370161.6:c.4699_4700insCACAACTAAAAGAAC	ENSP00000359180.2:n.4699_4700insCACAACTAAAAGAAC
ENST00000370163.7:c.*148_*149insCACAACTAAAAGAAC	ENSP00000359182.3:n.*148_*149insCACAACTAAAAGAAC
ENST00000370165.7:c.*148_*149insCACAACTAAAAGAAC	ENSP00000359184.3:n.*148_*149insCACAACTAAAAGAAC
NM_000028.2:c.*148_*149insCACAACTAAAAGAAC	NP_000019.2:n.*148_*149insCACAACTAAAAGAAC
NM_000642.2:c.*148_*149insCACAACTAAAAGAAC	NP_000633.2:n.*148_*149insCACAACTAAAAGAAC
NM_000643.2:c.*148_*149insCACAACTAAAAGAAC	NP_000634.2:n.*148_*149insCACAACTAAAAGAAC
NM_000644.2:c.*148_*149insCACAACTAAAAGAAC	NP_000635.2:n.*148_*149insCACAACTAAAAGAAC
NM_000645.2:c.*148_*149insCACAACTAAAAGAAC	NP_000636.2:n.*148_*149insCACAACTAAAAGAAC
NM_000646.2:c.*148_*149insCACAACTAAAAGAAC	NP_000637.2:n.*148_*149insCACAACTAAAAGAAC
XM_005270557.1:c.*148_*149insCACAACTAAAAGAAC	XP_005270614.1:n.*148_*149insCACAACTAAAAGAAC
XR_947626.1:n.1317+2438_1317+2439insGTTCTTTTAGTTGTG
XR_947627.1:n.1206+2438_1206+2439insGTTCTTTTAGTTGTG
XR_947628.1:n.1311+2438_1311+2439insGTTCTTTTAGTTGTG
XR_947630.1:n.1249+2438_1249+2439insGTTCTTTTAGTTGTG
XR_947632.1:n.1135+2438_1135+2439insGTTCTTTTAGTTGTG
XR_947633.1:n.1246+2438_1246+2439insGTTCTTTTAGTTGTG
XR_947634.1:n.660+2438_660+2439insGTTCTTTTAGTTGTG
XR_947635.1:n.728+2438_728+2439insGTTCTTTTAGTTGTG
XM_005270557.2:c.*148_*149insCACAACTAAAAGAAC	XP_005270614.1:n.*148_*149insCACAACTAAAAGAAC
XM_017000501.2:c.*148_*149insCACAACTAAAAGAAC	XP_016855990.1:n.*148_*149insCACAACTAAAAGAAC
NM_000642.3:c.*148_*149insCACAACTAAAAGAAC MANE Select	NP_000633.2:n.*148_*149insCACAACTAAAAGAAC