Canonical Allele Identifier: CA2646739560

Gene: AGL

Linked Data

• gnomAD v4: 1-99921697-A-ATCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921697_99921698insTCCT , CM000663.2:g.99921697_99921698insTCCT	GRCh38
NC_000001.10:g.100387253_100387254insTCCT , CM000663.1:g.100387253_100387254insTCCT	GRCh37
NC_000001.9:g.100159841_100159842insTCCT	NCBI36
NG_012865.1:g.76614_76615insTCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.*46_*47insTCCT MANE Select	ENSP00000355106.3:n.*46_*47insTCCT
ENST00000637337.1:n.4856_4857insTCCT
ENST00000294724.8:c.*46_*47insTCCT	ENSP00000294724.4:n.*46_*47insTCCT
ENST00000361302.7:c.*46_*47insTCCT	ENSP00000354971.3:n.*46_*47insTCCT
ENST00000361522.4:c.*46_*47insTCCT	ENSP00000354635.4:n.*46_*47insTCCT
ENST00000361915.7:c.*46_*47insTCCT	ENSP00000355106.3:n.*46_*47insTCCT
ENST00000370161.6:c.4597_4598insTCCT	ENSP00000359180.2:n.4597_4598insTCCT
ENST00000370163.7:c.*46_*47insTCCT	ENSP00000359182.3:n.*46_*47insTCCT
ENST00000370165.7:c.*46_*47insTCCT	ENSP00000359184.3:n.*46_*47insTCCT
NM_000028.2:c.*46_*47insTCCT	NP_000019.2:n.*46_*47insTCCT
NM_000642.2:c.*46_*47insTCCT	NP_000633.2:n.*46_*47insTCCT
NM_000643.2:c.*46_*47insTCCT	NP_000634.2:n.*46_*47insTCCT
NM_000644.2:c.*46_*47insTCCT	NP_000635.2:n.*46_*47insTCCT
NM_000645.2:c.*46_*47insTCCT	NP_000636.2:n.*46_*47insTCCT
NM_000646.2:c.*46_*47insTCCT	NP_000637.2:n.*46_*47insTCCT
XM_005270557.1:c.*46_*47insTCCT	XP_005270614.1:n.*46_*47insTCCT
XR_947626.1:n.1317+2540_1317+2541insAGGA
XR_947627.1:n.1206+2540_1206+2541insAGGA
XR_947628.1:n.1311+2540_1311+2541insAGGA
XR_947630.1:n.1249+2540_1249+2541insAGGA
XR_947632.1:n.1135+2540_1135+2541insAGGA
XR_947633.1:n.1246+2540_1246+2541insAGGA
XR_947634.1:n.660+2540_660+2541insAGGA
XR_947635.1:n.728+2540_728+2541insAGGA
XM_005270557.2:c.*46_*47insTCCT	XP_005270614.1:n.*46_*47insTCCT
XM_017000501.2:c.*46_*47insTCCT	XP_016855990.1:n.*46_*47insTCCT
NM_000642.3:c.*46_*47insTCCT MANE Select	NP_000633.2:n.*46_*47insTCCT