Canonical Allele Identifier: CA1183923206

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99870533C= , CM000663.2:g.99870533C=	GRCh38
NC_000001.10:g.100336089C= , CM000663.1:g.100336089C=	GRCh37
NC_000001.9:g.100108677C=	NCBI36
NG_012865.1:g.25450C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.798C= MANE Select	ENSP00000355106.3:p.Tyr266=
ENST00000637337.1:n.1009C=
ENST00000294724.8:c.798C=	ENSP00000294724.4:p.Tyr266=
ENST00000361302.7:c.750C=	ENSP00000354971.3:p.Tyr250=
ENST00000361522.4:c.747C=	ENSP00000354635.4:p.Tyr249=
ENST00000361915.7:c.798C=	ENSP00000355106.3:p.Tyr266=
ENST00000370161.6:c.750C=	ENSP00000359180.2:p.Tyr250=
ENST00000370163.7:c.798C=	ENSP00000359182.3:p.Tyr266=
ENST00000370165.7:c.798C=	ENSP00000359184.3:p.Tyr266=
NM_000028.2:c.798C=	NP_000019.2:p.Tyr266=
NM_000642.2:c.798C=	NP_000633.2:p.Tyr266=
NM_000643.2:c.798C=	NP_000634.2:p.Tyr266=
NM_000644.2:c.798C=	NP_000635.2:p.Tyr266=
NM_000645.2:c.747C=	NP_000636.2:p.Tyr249=
NM_000646.2:c.750C=	NP_000637.2:p.Tyr250=
XM_005270557.1:c.798C=	XP_005270614.1:p.Tyr266=
XM_005270557.2:c.798C=	XP_005270614.1:p.Tyr266=
NM_000642.3:c.798C= MANE Select	NP_000633.2:p.Tyr266=