Canonical Allele Identifier: CA1183944988

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921651_99921652delinsGT , CM000663.2:g.99921651_99921652delinsGT	GRCh38
NC_000001.10:g.100387207_100387208delinsGT , CM000663.1:g.100387207_100387208delinsGT	GRCh37
NC_000001.9:g.100159795_100159796delinsGT	NCBI36
NG_012865.1:g.76568_76569delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4599_*1delinsGT MANE Select	ENSP00000355106.3:n.[c.4599_*1delinsGT;Ter1533=]
ENST00000637337.1:n.4810_4811delinsGT
ENST00000294724.8:c.4599_*1delinsGT	ENSP00000294724.4:n.[c.4599_*1delinsGT;Ter1533=]
ENST00000361302.7:c.4551_*1delinsGT	ENSP00000354971.3:n.[c.4551_*1delinsGT;Ter1517=]
ENST00000361522.4:c.4548_*1delinsGT	ENSP00000354635.4:n.[c.4548_*1delinsGT;Ter1516=]
ENST00000361915.7:c.4599_*1delinsGT	ENSP00000355106.3:n.[c.4599_*1delinsGT;Ter1533=]
ENST00000370161.6:c.4551_4552delinsGT	ENSP00000359180.2:n.[c.4551_4552delinsGT;Ter1517=]
ENST00000370163.7:c.4599_*1delinsGT	ENSP00000359182.3:n.[c.4599_*1delinsGT;Ter1533=]
ENST00000370165.7:c.4599_*1delinsGT	ENSP00000359184.3:n.[c.4599_*1delinsGT;Ter1533=]
NM_000028.2:c.4599_*1delinsGT	NP_000019.2:n.[c.4599_*1delinsGT;Ter1533=]
NM_000642.2:c.4599_*1delinsGT	NP_000633.2:n.[c.4599_*1delinsGT;Ter1533=]
NM_000643.2:c.4599_*1delinsGT	NP_000634.2:n.[c.4599_*1delinsGT;Ter1533=]
NM_000644.2:c.4599_*1delinsGT	NP_000635.2:n.[c.4599_*1delinsGT;Ter1533=]
NM_000645.2:c.4548_*1delinsGT	NP_000636.2:n.[c.4548_*1delinsGT;Ter1516=]
NM_000646.2:c.4551_*1delinsGT	NP_000637.2:n.[c.4551_*1delinsGT;Ter1517=]
XM_005270557.1:c.4599_*1delinsGT	XP_005270614.1:n.[c.4599_*1delinsGT;Ter1533=]
XR_947626.1:n.1317+2586_1317+2587delinsAC
XR_947627.1:n.1206+2586_1206+2587delinsAC
XR_947628.1:n.1311+2586_1311+2587delinsAC
XR_947630.1:n.1249+2586_1249+2587delinsAC
XR_947632.1:n.1135+2586_1135+2587delinsAC
XR_947633.1:n.1246+2586_1246+2587delinsAC
XR_947634.1:n.660+2586_660+2587delinsAC
XR_947635.1:n.728+2586_728+2587delinsAC
XM_005270557.2:c.4599_*1delinsGT	XP_005270614.1:n.[c.4599_*1delinsGT;Ter1533=]
XM_017000501.2:c.2859_*1delinsGT	XP_016855990.1:n.[c.2859_*1delinsGT;Ter953=]
NM_000642.3:c.4599_*1delinsGT MANE Select	NP_000633.2:n.[c.4599_*1delinsGT;Ter1533=]