Canonical Allele Identifier: CA1183944797

Gene: AGL

Linked Data

• dbSNP Id: rs1655505951
• gnomAD v4: 1-99921491-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921491_99921492insT , CM000663.2:g.99921491_99921492insT	GRCh38
NC_000001.10:g.100387047_100387048insT , CM000663.1:g.100387047_100387048insT	GRCh37
NC_000001.9:g.100159635_100159636insT	NCBI36
NG_012865.1:g.76408_76409insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.4482-43_4482-42insT MANE Select	ENSP00000355106.3:n.4482-43_4482-42insT
ENST00000637337.1:n.4693-43_4693-42insT
ENST00000294724.8:c.4482-43_4482-42insT	ENSP00000294724.4:n.4482-43_4482-42insT
ENST00000361302.7:c.4434-43_4434-42insT	ENSP00000354971.3:n.4434-43_4434-42insT
ENST00000361522.4:c.4431-43_4431-42insT	ENSP00000354635.4:n.4431-43_4431-42insT
ENST00000361915.7:c.4482-43_4482-42insT	ENSP00000355106.3:n.4482-43_4482-42insT
ENST00000370161.6:c.4434-43_4434-42insT	ENSP00000359180.2:n.4434-43_4434-42insT
ENST00000370163.7:c.4482-43_4482-42insT	ENSP00000359182.3:n.4482-43_4482-42insT
ENST00000370165.7:c.4482-43_4482-42insT	ENSP00000359184.3:n.4482-43_4482-42insT
NM_000028.2:c.4482-43_4482-42insT	NP_000019.2:n.4482-43_4482-42insT
NM_000642.2:c.4482-43_4482-42insT	NP_000633.2:n.4482-43_4482-42insT
NM_000643.2:c.4482-43_4482-42insT	NP_000634.2:n.4482-43_4482-42insT
NM_000644.2:c.4482-43_4482-42insT	NP_000635.2:n.4482-43_4482-42insT
NM_000645.2:c.4431-43_4431-42insT	NP_000636.2:n.4431-43_4431-42insT
NM_000646.2:c.4434-43_4434-42insT	NP_000637.2:n.4434-43_4434-42insT
XM_005270557.1:c.4482-43_4482-42insT	XP_005270614.1:n.4482-43_4482-42insT
XR_947626.1:n.1317+2746_1317+2747insA
XR_947627.1:n.1206+2746_1206+2747insA
XR_947628.1:n.1311+2746_1311+2747insA
XR_947630.1:n.1249+2746_1249+2747insA
XR_947632.1:n.1135+2746_1135+2747insA
XR_947633.1:n.1246+2746_1246+2747insA
XR_947634.1:n.660+2746_660+2747insA
XR_947635.1:n.728+2746_728+2747insA
XM_005270557.2:c.4482-43_4482-42insT	XP_005270614.1:n.4482-43_4482-42insT
XM_017000501.2:c.2742-43_2742-42insT	XP_016855990.1:n.2742-43_2742-42insT
NM_000642.3:c.4482-43_4482-42insT MANE Select	NP_000633.2:n.4482-43_4482-42insT