Canonical Allele Identifier: CA1183944738

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921402_99921405delinsATTG , CM000663.2:g.99921402_99921405delinsATTG	GRCh38
NC_000001.10:g.100386958_100386961delinsATTG , CM000663.1:g.100386958_100386961delinsATTG	GRCh37
NC_000001.9:g.100159546_100159549delinsATTG	NCBI36
NG_012865.1:g.76319_76322delinsATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4482-132_4482-129delinsATTG MANE Select	ENSP00000355106.3:n.4482-132_4482-129delinsATTG
ENST00000637337.1:n.4693-132_4693-129delinsATTG
ENST00000294724.8:c.4482-132_4482-129delinsATTG	ENSP00000294724.4:n.4482-132_4482-129delinsATTG
ENST00000361302.7:c.4434-132_4434-129delinsATTG	ENSP00000354971.3:n.4434-132_4434-129delinsATTG
ENST00000361522.4:c.4431-132_4431-129delinsATTG	ENSP00000354635.4:n.4431-132_4431-129delinsATTG
ENST00000361915.7:c.4482-132_4482-129delinsATTG	ENSP00000355106.3:n.4482-132_4482-129delinsATTG
ENST00000370161.6:c.4434-132_4434-129delinsATTG	ENSP00000359180.2:n.4434-132_4434-129delinsATTG
ENST00000370163.7:c.4482-132_4482-129delinsATTG	ENSP00000359182.3:n.4482-132_4482-129delinsATTG
ENST00000370165.7:c.4482-132_4482-129delinsATTG	ENSP00000359184.3:n.4482-132_4482-129delinsATTG
NM_000028.2:c.4482-132_4482-129delinsATTG	NP_000019.2:n.4482-132_4482-129delinsATTG
NM_000642.2:c.4482-132_4482-129delinsATTG	NP_000633.2:n.4482-132_4482-129delinsATTG
NM_000643.2:c.4482-132_4482-129delinsATTG	NP_000634.2:n.4482-132_4482-129delinsATTG
NM_000644.2:c.4482-132_4482-129delinsATTG	NP_000635.2:n.4482-132_4482-129delinsATTG
NM_000645.2:c.4431-132_4431-129delinsATTG	NP_000636.2:n.4431-132_4431-129delinsATTG
NM_000646.2:c.4434-132_4434-129delinsATTG	NP_000637.2:n.4434-132_4434-129delinsATTG
XM_005270557.1:c.4482-132_4482-129delinsATTG	XP_005270614.1:n.4482-132_4482-129delinsATTG
XR_947626.1:n.1317+2833_1317+2836delinsCAAT
XR_947627.1:n.1206+2833_1206+2836delinsCAAT
XR_947628.1:n.1311+2833_1311+2836delinsCAAT
XR_947630.1:n.1249+2833_1249+2836delinsCAAT
XR_947632.1:n.1135+2833_1135+2836delinsCAAT
XR_947633.1:n.1246+2833_1246+2836delinsCAAT
XR_947634.1:n.660+2833_660+2836delinsCAAT
XR_947635.1:n.728+2833_728+2836delinsCAAT
XM_005270557.2:c.4482-132_4482-129delinsATTG	XP_005270614.1:n.4482-132_4482-129delinsATTG
XM_017000501.2:c.2742-132_2742-129delinsATTG	XP_016855990.1:n.2742-132_2742-129delinsATTG
NM_000642.3:c.4482-132_4482-129delinsATTG MANE Select	NP_000633.2:n.4482-132_4482-129delinsATTG