Canonical Allele Identifier: CA1183937269

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99900730G= , CM000663.2:g.99900730G=	GRCh38
NC_000001.10:g.100366286G= , CM000663.1:g.100366286G=	GRCh37
NC_000001.9:g.100138874G=	NCBI36
NG_012865.1:g.55647G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.3457G= MANE Select	ENSP00000355106.3:p.Ala1153=
ENST00000637337.1:n.3668G=
ENST00000294724.8:c.3457G=	ENSP00000294724.4:p.Ala1153=
ENST00000361302.7:c.3409G=	ENSP00000354971.3:p.Ala1137=
ENST00000361522.4:c.3406G=	ENSP00000354635.4:p.Ala1136=
ENST00000361915.7:c.3457G=	ENSP00000355106.3:p.Ala1153=
ENST00000370161.6:c.3409G=	ENSP00000359180.2:p.Ala1137=
ENST00000370163.7:c.3457G=	ENSP00000359182.3:p.Ala1153=
ENST00000370165.7:c.3457G=	ENSP00000359184.3:p.Ala1153=
NM_000028.2:c.3457G=	NP_000019.2:p.Ala1153=
NM_000642.2:c.3457G=	NP_000633.2:p.Ala1153=
NM_000643.2:c.3457G=	NP_000634.2:p.Ala1153=
NM_000644.2:c.3457G=	NP_000635.2:p.Ala1153=
NM_000645.2:c.3406G=	NP_000636.2:p.Ala1136=
NM_000646.2:c.3409G=	NP_000637.2:p.Ala1137=
XM_005270557.1:c.3457G=	XP_005270614.1:p.Ala1153=
XM_005270557.2:c.3457G=	XP_005270614.1:p.Ala1153=
XM_017000501.2:c.1717G=	XP_016855990.1:p.Ala573=
NM_000642.3:c.3457G= MANE Select	NP_000633.2:p.Ala1153=