Canonical Allele Identifier: CA1183941832

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99910976_99910977delinsCT , CM000663.2:g.99910976_99910977delinsCT	GRCh38
NC_000001.10:g.100376532_100376533delinsCT , CM000663.1:g.100376532_100376533delinsCT	GRCh37
NC_000001.9:g.100149120_100149121delinsCT	NCBI36
NG_012865.1:g.65893_65894delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.3836+129_3836+130delinsCT MANE Select	ENSP00000355106.3:n.3836+129_3836+130delinsCT
ENST00000637337.1:n.4047+129_4047+130delinsCT
ENST00000294724.8:c.3836+129_3836+130delinsCT	ENSP00000294724.4:n.3836+129_3836+130delinsCT
ENST00000361302.7:c.3788+129_3788+130delinsCT	ENSP00000354971.3:n.3788+129_3788+130delinsCT
ENST00000361522.4:c.3785+129_3785+130delinsCT	ENSP00000354635.4:n.3785+129_3785+130delinsCT
ENST00000361915.7:c.3836+129_3836+130delinsCT	ENSP00000355106.3:n.3836+129_3836+130delinsCT
ENST00000370161.6:c.3788+129_3788+130delinsCT	ENSP00000359180.2:n.3788+129_3788+130delinsCT
ENST00000370163.7:c.3836+129_3836+130delinsCT	ENSP00000359182.3:n.3836+129_3836+130delinsCT
ENST00000370165.7:c.3836+129_3836+130delinsCT	ENSP00000359184.3:n.3836+129_3836+130delinsCT
NM_000028.2:c.3836+129_3836+130delinsCT	NP_000019.2:n.3836+129_3836+130delinsCT
NM_000642.2:c.3836+129_3836+130delinsCT	NP_000633.2:n.3836+129_3836+130delinsCT
NM_000643.2:c.3836+129_3836+130delinsCT	NP_000634.2:n.3836+129_3836+130delinsCT
NM_000644.2:c.3836+129_3836+130delinsCT	NP_000635.2:n.3836+129_3836+130delinsCT
NM_000645.2:c.3785+129_3785+130delinsCT	NP_000636.2:n.3785+129_3785+130delinsCT
NM_000646.2:c.3788+129_3788+130delinsCT	NP_000637.2:n.3788+129_3788+130delinsCT
XM_005270557.1:c.3836+129_3836+130delinsCT	XP_005270614.1:n.3836+129_3836+130delinsCT
XM_005270557.2:c.3836+129_3836+130delinsCT	XP_005270614.1:n.3836+129_3836+130delinsCT
XM_017000501.2:c.2096+129_2096+130delinsCT	XP_016855990.1:n.2096+129_2096+130delinsCT
NM_000642.3:c.3836+129_3836+130delinsCT MANE Select	NP_000633.2:n.3836+129_3836+130delinsCT