Canonical Allele Identifier: CA1183941666

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99916671_99916672delinsCT , CM000663.2:g.99916671_99916672delinsCT	GRCh38
NC_000001.10:g.100382227_100382228delinsCT , CM000663.1:g.100382227_100382228delinsCT	GRCh37
NC_000001.9:g.100154815_100154816delinsCT	NCBI36
NG_012865.1:g.71588_71589delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4421_4422delinsCT MANE Select	ENSP00000355106.3:p.Thr1474=
ENST00000637337.1:n.4632_4633delinsCT
ENST00000294724.8:c.4421_4422delinsCT	ENSP00000294724.4:p.Thr1474=
ENST00000361302.7:c.4373_4374delinsCT	ENSP00000354971.3:p.Thr1458=
ENST00000361522.4:c.4370_4371delinsCT	ENSP00000354635.4:p.Thr1457=
ENST00000361915.7:c.4421_4422delinsCT	ENSP00000355106.3:p.Thr1474=
ENST00000370161.6:c.4373_4374delinsCT	ENSP00000359180.2:p.Thr1458=
ENST00000370163.7:c.4421_4422delinsCT	ENSP00000359182.3:p.Thr1474=
ENST00000370165.7:c.4421_4422delinsCT	ENSP00000359184.3:p.Thr1474=
NM_000028.2:c.4421_4422delinsCT	NP_000019.2:p.Thr1474=
NM_000642.2:c.4421_4422delinsCT	NP_000633.2:p.Thr1474=
NM_000643.2:c.4421_4422delinsCT	NP_000634.2:p.Thr1474=
NM_000644.2:c.4421_4422delinsCT	NP_000635.2:p.Thr1474=
NM_000645.2:c.4370_4371delinsCT	NP_000636.2:p.Thr1457=
NM_000646.2:c.4373_4374delinsCT	NP_000637.2:p.Thr1458=
XM_005270557.1:c.4421_4422delinsCT	XP_005270614.1:p.Thr1474=
XR_947626.1:n.1318-3455_1318-3454delinsAG
XR_947627.1:n.1207-3455_1207-3454delinsAG
XR_947628.1:n.1312-3455_1312-3454delinsAG
XR_947630.1:n.1250-3455_1250-3454delinsAG
XR_947632.1:n.1136-3455_1136-3454delinsAG
XR_947633.1:n.1247-3455_1247-3454delinsAG
XR_947634.1:n.661-3455_661-3454delinsAG
XR_947635.1:n.729-3455_729-3454delinsAG
XM_005270557.2:c.4421_4422delinsCT	XP_005270614.1:p.Thr1474=
XM_017000501.2:c.2681_2682delinsCT	XP_016855990.1:p.Thr894=
NM_000642.3:c.4421_4422delinsCT MANE Select	NP_000633.2:p.Thr1474=