Canonical Allele Identifier: CA2744753402

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921877_99921878insCTG , CM000663.2:g.99921877_99921878insCTG	GRCh38
NC_000001.10:g.100387433_100387434insCTG , CM000663.1:g.100387433_100387434insCTG	GRCh37
NC_000001.9:g.100160021_100160022insCTG	NCBI36
NG_012865.1:g.76794_76795insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.*226_*227insCTG MANE Select	ENSP00000355106.3:n.*226_*227insCTG
ENST00000637337.1:n.5036_5037insCTG
ENST00000294724.8:c.*226_*227insCTG	ENSP00000294724.4:n.*226_*227insCTG
ENST00000361302.7:c.*226_*227insCTG	ENSP00000354971.3:n.*226_*227insCTG
ENST00000361522.4:c.*226_*227insCTG	ENSP00000354635.4:n.*226_*227insCTG
ENST00000361915.7:c.*226_*227insCTG	ENSP00000355106.3:n.*226_*227insCTG
ENST00000370161.6:c.4777_4778insCTG	ENSP00000359180.2:n.4777_4778insCTG
ENST00000370163.7:c.*226_*227insCTG	ENSP00000359182.3:n.*226_*227insCTG
ENST00000370165.7:c.*226_*227insCTG	ENSP00000359184.3:n.*226_*227insCTG
NM_000028.2:c.*226_*227insCTG	NP_000019.2:n.*226_*227insCTG
NM_000642.2:c.*226_*227insCTG	NP_000633.2:n.*226_*227insCTG
NM_000643.2:c.*226_*227insCTG	NP_000634.2:n.*226_*227insCTG
NM_000644.2:c.*226_*227insCTG	NP_000635.2:n.*226_*227insCTG
NM_000645.2:c.*226_*227insCTG	NP_000636.2:n.*226_*227insCTG
NM_000646.2:c.*226_*227insCTG	NP_000637.2:n.*226_*227insCTG
XM_005270557.1:c.*226_*227insCTG	XP_005270614.1:n.*226_*227insCTG
XR_947626.1:n.1317+2360_1317+2361insCAG
XR_947627.1:n.1206+2360_1206+2361insCAG
XR_947628.1:n.1311+2360_1311+2361insCAG
XR_947630.1:n.1249+2360_1249+2361insCAG
XR_947632.1:n.1135+2360_1135+2361insCAG
XR_947633.1:n.1246+2360_1246+2361insCAG
XR_947634.1:n.660+2360_660+2361insCAG
XR_947635.1:n.728+2360_728+2361insCAG
XM_005270557.2:c.*226_*227insCTG	XP_005270614.1:n.*226_*227insCTG
XM_017000501.2:c.*226_*227insCTG	XP_016855990.1:n.*226_*227insCTG
NM_000642.3:c.*226_*227insCTG MANE Select	NP_000633.2:n.*226_*227insCTG