Canonical Allele Identifier: CA1183946653

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99916374_99916377delinsATCT , CM000663.2:g.99916374_99916377delinsATCT	GRCh38
NC_000001.10:g.100381930_100381933delinsATCT , CM000663.1:g.100381930_100381933delinsATCT	GRCh37
NC_000001.9:g.100154518_100154521delinsATCT	NCBI36
NG_012865.1:g.71291_71294delinsATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4260-36_4260-33delinsATCT MANE Select	ENSP00000355106.3:n.4260-36_4260-33delinsATCT
ENST00000637337.1:n.4471-36_4471-33delinsATCT
ENST00000294724.8:c.4260-36_4260-33delinsATCT	ENSP00000294724.4:n.4260-36_4260-33delinsATCT
ENST00000361302.7:c.4212-36_4212-33delinsATCT	ENSP00000354971.3:n.4212-36_4212-33delinsATCT
ENST00000361522.4:c.4209-36_4209-33delinsATCT	ENSP00000354635.4:n.4209-36_4209-33delinsATCT
ENST00000361915.7:c.4260-36_4260-33delinsATCT	ENSP00000355106.3:n.4260-36_4260-33delinsATCT
ENST00000370161.6:c.4212-36_4212-33delinsATCT	ENSP00000359180.2:n.4212-36_4212-33delinsATCT
ENST00000370163.7:c.4260-36_4260-33delinsATCT	ENSP00000359182.3:n.4260-36_4260-33delinsATCT
ENST00000370165.7:c.4260-36_4260-33delinsATCT	ENSP00000359184.3:n.4260-36_4260-33delinsATCT
NM_000028.2:c.4260-36_4260-33delinsATCT	NP_000019.2:n.4260-36_4260-33delinsATCT
NM_000642.2:c.4260-36_4260-33delinsATCT	NP_000633.2:n.4260-36_4260-33delinsATCT
NM_000643.2:c.4260-36_4260-33delinsATCT	NP_000634.2:n.4260-36_4260-33delinsATCT
NM_000644.2:c.4260-36_4260-33delinsATCT	NP_000635.2:n.4260-36_4260-33delinsATCT
NM_000645.2:c.4209-36_4209-33delinsATCT	NP_000636.2:n.4209-36_4209-33delinsATCT
NM_000646.2:c.4212-36_4212-33delinsATCT	NP_000637.2:n.4212-36_4212-33delinsATCT
XM_005270557.1:c.4260-36_4260-33delinsATCT	XP_005270614.1:n.4260-36_4260-33delinsATCT
XR_947626.1:n.1318-3160_1318-3157delinsAGAT
XR_947627.1:n.1207-3160_1207-3157delinsAGAT
XR_947628.1:n.1312-3160_1312-3157delinsAGAT
XR_947630.1:n.1250-3160_1250-3157delinsAGAT
XR_947632.1:n.1136-3160_1136-3157delinsAGAT
XR_947633.1:n.1247-3160_1247-3157delinsAGAT
XR_947634.1:n.661-3160_661-3157delinsAGAT
XR_947635.1:n.729-3160_729-3157delinsAGAT
XM_005270557.2:c.4260-36_4260-33delinsATCT	XP_005270614.1:n.4260-36_4260-33delinsATCT
XM_017000501.2:c.2520-36_2520-33delinsATCT	XP_016855990.1:n.2520-36_2520-33delinsATCT
NM_000642.3:c.4260-36_4260-33delinsATCT MANE Select	NP_000633.2:n.4260-36_4260-33delinsATCT