Canonical Allele Identifier: CA1183945211

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921936_99921939delinsATCT , CM000663.2:g.99921936_99921939delinsATCT	GRCh38
NC_000001.10:g.100387492_100387495delinsATCT , CM000663.1:g.100387492_100387495delinsATCT	GRCh37
NC_000001.9:g.100160080_100160083delinsATCT	NCBI36
NG_012865.1:g.76853_76856delinsATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.*285_*288delinsATCT MANE Select	ENSP00000355106.3:n.*285_*288delinsATCT
ENST00000637337.1:n.5095_5098delinsATCT
ENST00000294724.8:c.*285_*288delinsATCT	ENSP00000294724.4:n.*285_*288delinsATCT
ENST00000361302.7:c.*285_*288delinsATCT	ENSP00000354971.3:n.*285_*288delinsATCT
ENST00000361522.4:c.*285_*288delinsATCT	ENSP00000354635.4:n.*285_*288delinsATCT
ENST00000361915.7:c.*285_*288delinsATCT	ENSP00000355106.3:n.*285_*288delinsATCT
ENST00000370161.6:c.4836_4839delinsATCT	ENSP00000359180.2:n.4836_4839delinsATCT
ENST00000370163.7:c.*285_*288delinsATCT	ENSP00000359182.3:n.*285_*288delinsATCT
ENST00000370165.7:c.*285_*288delinsATCT	ENSP00000359184.3:n.*285_*288delinsATCT
NM_000028.2:c.*285_*288delinsATCT	NP_000019.2:n.*285_*288delinsATCT
NM_000642.2:c.*285_*288delinsATCT	NP_000633.2:n.*285_*288delinsATCT
NM_000643.2:c.*285_*288delinsATCT	NP_000634.2:n.*285_*288delinsATCT
NM_000644.2:c.*285_*288delinsATCT	NP_000635.2:n.*285_*288delinsATCT
NM_000645.2:c.*285_*288delinsATCT	NP_000636.2:n.*285_*288delinsATCT
NM_000646.2:c.*285_*288delinsATCT	NP_000637.2:n.*285_*288delinsATCT
XM_005270557.1:c.*285_*288delinsATCT	XP_005270614.1:n.*285_*288delinsATCT
XR_947626.1:n.1317+2299_1317+2302delinsAGAT
XR_947627.1:n.1206+2299_1206+2302delinsAGAT
XR_947628.1:n.1311+2299_1311+2302delinsAGAT
XR_947630.1:n.1249+2299_1249+2302delinsAGAT
XR_947632.1:n.1135+2299_1135+2302delinsAGAT
XR_947633.1:n.1246+2299_1246+2302delinsAGAT
XR_947634.1:n.660+2299_660+2302delinsAGAT
XR_947635.1:n.728+2299_728+2302delinsAGAT
XM_005270557.2:c.*285_*288delinsATCT	XP_005270614.1:n.*285_*288delinsATCT
XM_017000501.2:c.*285_*288delinsATCT	XP_016855990.1:n.*285_*288delinsATCT
NM_000642.3:c.*285_*288delinsATCT MANE Select	NP_000633.2:n.*285_*288delinsATCT