Canonical Allele Identifier: CA2574444576

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99880689_99880691del , CM000663.2:g.99880689_99880691del	GRCh38
NC_000001.10:g.100346245_100346247del , CM000663.1:g.100346245_100346247del	GRCh37
NC_000001.9:g.100118833_100118835del	NCBI36
NG_012865.1:g.35606_35608del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.1793_1795del MANE Select	ENSP00000355106.3:p.Gly598del
ENST00000637337.1:n.2004_2006del
ENST00000294724.8:c.1793_1795del	ENSP00000294724.4:p.Gly598del
ENST00000361302.7:c.1745_1747del	ENSP00000354971.3:p.Gly582del
ENST00000361522.4:c.1742_1744del	ENSP00000354635.4:p.Gly581del
ENST00000361915.7:c.1793_1795del	ENSP00000355106.3:p.Gly598del
ENST00000370161.6:c.1745_1747del	ENSP00000359180.2:p.Gly582del
ENST00000370163.7:c.1793_1795del	ENSP00000359182.3:p.Gly598del
ENST00000370165.7:c.1793_1795del	ENSP00000359184.3:p.Gly598del
NM_000028.2:c.1793_1795del	NP_000019.2:p.Gly598del
NM_000642.2:c.1793_1795del	NP_000633.2:p.Gly598del
NM_000643.2:c.1793_1795del	NP_000634.2:p.Gly598del
NM_000644.2:c.1793_1795del	NP_000635.2:p.Gly598del
NM_000645.2:c.1742_1744del	NP_000636.2:p.Gly581del
NM_000646.2:c.1745_1747del	NP_000637.2:p.Gly582del
XM_005270557.1:c.1793_1795del	XP_005270614.1:p.Gly598del
XM_005270557.2:c.1793_1795del	XP_005270614.1:p.Gly598del
XM_017000501.2:c.53_55del	XP_016855990.1:p.Gly18del
NM_000642.3:c.1793_1795del MANE Select	NP_000633.2:p.Gly598del