Canonical Allele Identifier: CA1183944942

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921622A= , CM000663.2:g.99921622A=	GRCh38
NC_000001.10:g.100387178A= , CM000663.1:g.100387178A=	GRCh37
NC_000001.9:g.100159766A=	NCBI36
NG_012865.1:g.76539A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4570A= MANE Select	ENSP00000355106.3:p.Thr1524=
ENST00000637337.1:n.4781A=
ENST00000294724.8:c.4570A=	ENSP00000294724.4:p.Thr1524=
ENST00000361302.7:c.4522A=	ENSP00000354971.3:p.Thr1508=
ENST00000361522.4:c.4519A=	ENSP00000354635.4:p.Thr1507=
ENST00000361915.7:c.4570A=	ENSP00000355106.3:p.Thr1524=
ENST00000370161.6:c.4522A=	ENSP00000359180.2:p.Thr1508=
ENST00000370163.7:c.4570A=	ENSP00000359182.3:p.Thr1524=
ENST00000370165.7:c.4570A=	ENSP00000359184.3:p.Thr1524=
NM_000028.2:c.4570A=	NP_000019.2:p.Thr1524=
NM_000642.2:c.4570A=	NP_000633.2:p.Thr1524=
NM_000643.2:c.4570A=	NP_000634.2:p.Thr1524=
NM_000644.2:c.4570A=	NP_000635.2:p.Thr1524=
NM_000645.2:c.4519A=	NP_000636.2:p.Thr1507=
NM_000646.2:c.4522A=	NP_000637.2:p.Thr1508=
XM_005270557.1:c.4570A=	XP_005270614.1:p.Thr1524=
XR_947626.1:n.1317+2616T=
XR_947627.1:n.1206+2616T=
XR_947628.1:n.1311+2616T=
XR_947630.1:n.1249+2616T=
XR_947632.1:n.1135+2616T=
XR_947633.1:n.1246+2616T=
XR_947634.1:n.660+2616T=
XR_947635.1:n.728+2616T=
XM_005270557.2:c.4570A=	XP_005270614.1:p.Thr1524=
XM_017000501.2:c.2830A=	XP_016855990.1:p.Thr944=
NM_000642.3:c.4570A= MANE Select	NP_000633.2:p.Thr1524=