Canonical Allele Identifier: CA1183944812

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921505_99921506delinsCT , CM000663.2:g.99921505_99921506delinsCT	GRCh38
NC_000001.10:g.100387061_100387062delinsCT , CM000663.1:g.100387061_100387062delinsCT	GRCh37
NC_000001.9:g.100159649_100159650delinsCT	NCBI36
NG_012865.1:g.76422_76423delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.4482-29_4482-28delinsCT MANE Select	ENSP00000355106.3:n.4482-29_4482-28delins...
ENST00000637337.1:n.4693-29_4693-28delinsCT
ENST00000294724.8:c.4482-29_4482-28delinsCT	ENSP00000294724.4:n.4482-29_4482-28delins...
ENST00000361302.7:c.4434-29_4434-28delinsCT	ENSP00000354971.3:n.4434-29_4434-28delins...
ENST00000361522.4:c.4431-29_4431-28delinsCT	ENSP00000354635.4:n.4431-29_4431-28delins...
ENST00000361915.7:c.4482-29_4482-28delinsCT	ENSP00000355106.3:n.4482-29_4482-28delins...
ENST00000370161.6:c.4434-29_4434-28delinsCT	ENSP00000359180.2:n.4434-29_4434-28delins...
ENST00000370163.7:c.4482-29_4482-28delinsCT	ENSP00000359182.3:n.4482-29_4482-28delins...
ENST00000370165.7:c.4482-29_4482-28delinsCT	ENSP00000359184.3:n.4482-29_4482-28delins...
NM_000028.2:c.4482-29_4482-28delinsCT	NP_000019.2:n.4482-29_4482-28delinsCT
NM_000642.2:c.4482-29_4482-28delinsCT	NP_000633.2:n.4482-29_4482-28delinsCT
NM_000643.2:c.4482-29_4482-28delinsCT	NP_000634.2:n.4482-29_4482-28delinsCT
NM_000644.2:c.4482-29_4482-28delinsCT	NP_000635.2:n.4482-29_4482-28delinsCT
NM_000645.2:c.4431-29_4431-28delinsCT	NP_000636.2:n.4431-29_4431-28delinsCT
NM_000646.2:c.4434-29_4434-28delinsCT	NP_000637.2:n.4434-29_4434-28delinsCT
XM_005270557.1:c.4482-29_4482-28delinsCT	XP_005270614.1:n.4482-29_4482-28delinsCT
XR_947626.1:n.1317+2732_1317+2733delinsAG
XR_947627.1:n.1206+2732_1206+2733delinsAG
XR_947628.1:n.1311+2732_1311+2733delinsAG
XR_947630.1:n.1249+2732_1249+2733delinsAG
XR_947632.1:n.1135+2732_1135+2733delinsAG
XR_947633.1:n.1246+2732_1246+2733delinsAG
XR_947634.1:n.660+2732_660+2733delinsAG
XR_947635.1:n.728+2732_728+2733delinsAG
XM_005270557.2:c.4482-29_4482-28delinsCT	XP_005270614.1:n.4482-29_4482-28delinsCT
XM_017000501.2:c.2742-29_2742-28delinsCT	XP_016855990.1:n.2742-29_2742-28delinsCT
NM_000642.3:c.4482-29_4482-28delinsCT MANE Select	NP_000633.2:n.4482-29_4482-28delinsCT