Canonical Allele Identifier: CA1183946664

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99916381_99916382delinsAT , CM000663.2:g.99916381_99916382delinsAT	GRCh38
NC_000001.10:g.100381937_100381938delinsAT , CM000663.1:g.100381937_100381938delinsAT	GRCh37
NC_000001.9:g.100154525_100154526delinsAT	NCBI36
NG_012865.1:g.71298_71299delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4260-29_4260-28delinsAT MANE Select	ENSP00000355106.3:n.4260-29_4260-28delinsAT
ENST00000637337.1:n.4471-29_4471-28delinsAT
ENST00000294724.8:c.4260-29_4260-28delinsAT	ENSP00000294724.4:n.4260-29_4260-28delinsAT
ENST00000361302.7:c.4212-29_4212-28delinsAT	ENSP00000354971.3:n.4212-29_4212-28delinsAT
ENST00000361522.4:c.4209-29_4209-28delinsAT	ENSP00000354635.4:n.4209-29_4209-28delinsAT
ENST00000361915.7:c.4260-29_4260-28delinsAT	ENSP00000355106.3:n.4260-29_4260-28delinsAT
ENST00000370161.6:c.4212-29_4212-28delinsAT	ENSP00000359180.2:n.4212-29_4212-28delinsAT
ENST00000370163.7:c.4260-29_4260-28delinsAT	ENSP00000359182.3:n.4260-29_4260-28delinsAT
ENST00000370165.7:c.4260-29_4260-28delinsAT	ENSP00000359184.3:n.4260-29_4260-28delinsAT
NM_000028.2:c.4260-29_4260-28delinsAT	NP_000019.2:n.4260-29_4260-28delinsAT
NM_000642.2:c.4260-29_4260-28delinsAT	NP_000633.2:n.4260-29_4260-28delinsAT
NM_000643.2:c.4260-29_4260-28delinsAT	NP_000634.2:n.4260-29_4260-28delinsAT
NM_000644.2:c.4260-29_4260-28delinsAT	NP_000635.2:n.4260-29_4260-28delinsAT
NM_000645.2:c.4209-29_4209-28delinsAT	NP_000636.2:n.4209-29_4209-28delinsAT
NM_000646.2:c.4212-29_4212-28delinsAT	NP_000637.2:n.4212-29_4212-28delinsAT
XM_005270557.1:c.4260-29_4260-28delinsAT	XP_005270614.1:n.4260-29_4260-28delinsAT
XR_947626.1:n.1318-3165_1318-3164delinsAT
XR_947627.1:n.1207-3165_1207-3164delinsAT
XR_947628.1:n.1312-3165_1312-3164delinsAT
XR_947630.1:n.1250-3165_1250-3164delinsAT
XR_947632.1:n.1136-3165_1136-3164delinsAT
XR_947633.1:n.1247-3165_1247-3164delinsAT
XR_947634.1:n.661-3165_661-3164delinsAT
XR_947635.1:n.729-3165_729-3164delinsAT
XM_005270557.2:c.4260-29_4260-28delinsAT	XP_005270614.1:n.4260-29_4260-28delinsAT
XM_017000501.2:c.2520-29_2520-28delinsAT	XP_016855990.1:n.2520-29_2520-28delinsAT
NM_000642.3:c.4260-29_4260-28delinsAT MANE Select	NP_000633.2:n.4260-29_4260-28delinsAT