Canonical Allele Identifier: CA2744753415

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921913_99921918del , CM000663.2:g.99921913_99921918del	GRCh38
NC_000001.10:g.100387469_100387474del , CM000663.1:g.100387469_100387474del	GRCh37
NC_000001.9:g.100160057_100160062del	NCBI36
NG_012865.1:g.76830_76835del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.*262_*267del MANE Select	ENSP00000355106.3:n.*262_*267del
ENST00000637337.1:n.5072_5077del
ENST00000294724.8:c.*262_*267del	ENSP00000294724.4:n.*262_*267del
ENST00000361302.7:c.*262_*267del	ENSP00000354971.3:n.*262_*267del
ENST00000361522.4:c.*262_*267del	ENSP00000354635.4:n.*262_*267del
ENST00000361915.7:c.*262_*267del	ENSP00000355106.3:n.*262_*267del
ENST00000370161.6:c.4813_4818del	ENSP00000359180.2:n.4813_4818del
ENST00000370163.7:c.*262_*267del	ENSP00000359182.3:n.*262_*267del
ENST00000370165.7:c.*262_*267del	ENSP00000359184.3:n.*262_*267del
NM_000028.2:c.*262_*267del	NP_000019.2:n.*262_*267del
NM_000642.2:c.*262_*267del	NP_000633.2:n.*262_*267del
NM_000643.2:c.*262_*267del	NP_000634.2:n.*262_*267del
NM_000644.2:c.*262_*267del	NP_000635.2:n.*262_*267del
NM_000645.2:c.*262_*267del	NP_000636.2:n.*262_*267del
NM_000646.2:c.*262_*267del	NP_000637.2:n.*262_*267del
XM_005270557.1:c.*262_*267del	XP_005270614.1:n.*262_*267del
XR_947626.1:n.1317+2320_1317+2325del
XR_947627.1:n.1206+2320_1206+2325del
XR_947628.1:n.1311+2320_1311+2325del
XR_947630.1:n.1249+2320_1249+2325del
XR_947632.1:n.1135+2320_1135+2325del
XR_947633.1:n.1246+2320_1246+2325del
XR_947634.1:n.660+2320_660+2325del
XR_947635.1:n.728+2320_728+2325del
XM_005270557.2:c.*262_*267del	XP_005270614.1:n.*262_*267del
XM_017000501.2:c.*262_*267del	XP_016855990.1:n.*262_*267del
NM_000642.3:c.*262_*267del MANE Select	NP_000633.2:n.*262_*267del