Canonical Allele Identifier: CA2744756003

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99896505_99896506insCTC , CM000663.2:g.99896505_99896506insCTC	GRCh38
NC_000001.10:g.100362061_100362062insCTC , CM000663.1:g.100362061_100362062insCTC	GRCh37
NC_000001.9:g.100134649_100134650insCTC	NCBI36
NG_012865.1:g.51422_51423insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.3362+117_3362+118insCTC MANE Select	ENSP00000355106.3:n.3362+117_3362+118insCTC
ENST00000637337.1:n.3573+117_3573+118insCTC
ENST00000294724.8:c.3362+117_3362+118insCTC	ENSP00000294724.4:n.3362+117_3362+118insCTC
ENST00000361302.7:c.3314+117_3314+118insCTC	ENSP00000354971.3:n.3314+117_3314+118insCTC
ENST00000361522.4:c.3311+117_3311+118insCTC	ENSP00000354635.4:n.3311+117_3311+118insCTC
ENST00000361915.7:c.3362+117_3362+118insCTC	ENSP00000355106.3:n.3362+117_3362+118insCTC
ENST00000370161.6:c.3314+117_3314+118insCTC	ENSP00000359180.2:n.3314+117_3314+118insCTC
ENST00000370163.7:c.3362+117_3362+118insCTC	ENSP00000359182.3:n.3362+117_3362+118insCTC
ENST00000370165.7:c.3362+117_3362+118insCTC	ENSP00000359184.3:n.3362+117_3362+118insCTC
NM_000028.2:c.3362+117_3362+118insCTC	NP_000019.2:n.3362+117_3362+118insCTC
NM_000642.2:c.3362+117_3362+118insCTC	NP_000633.2:n.3362+117_3362+118insCTC
NM_000643.2:c.3362+117_3362+118insCTC	NP_000634.2:n.3362+117_3362+118insCTC
NM_000644.2:c.3362+117_3362+118insCTC	NP_000635.2:n.3362+117_3362+118insCTC
NM_000645.2:c.3311+117_3311+118insCTC	NP_000636.2:n.3311+117_3311+118insCTC
NM_000646.2:c.3314+117_3314+118insCTC	NP_000637.2:n.3314+117_3314+118insCTC
XM_005270557.1:c.3362+117_3362+118insCTC	XP_005270614.1:n.3362+117_3362+118insCTC
XM_005270557.2:c.3362+117_3362+118insCTC	XP_005270614.1:n.3362+117_3362+118insCTC
XM_017000501.2:c.1622+117_1622+118insCTC	XP_016855990.1:n.1622+117_1622+118insCTC
NM_000642.3:c.3362+117_3362+118insCTC MANE Select	NP_000633.2:n.3362+117_3362+118insCTC