Canonical Allele Identifier: CA1183944921

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921604C= , CM000663.2:g.99921604C=	GRCh38
NC_000001.10:g.100387160C= , CM000663.1:g.100387160C=	GRCh37
NC_000001.9:g.100159748C=	NCBI36
NG_012865.1:g.76521C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.4552C= MANE Select	ENSP00000355106.3:p.Gln1518=
ENST00000637337.1:n.4763C=
ENST00000294724.8:c.4552C=	ENSP00000294724.4:p.Gln1518=
ENST00000361302.7:c.4504C=	ENSP00000354971.3:p.Gln1502=
ENST00000361522.4:c.4501C=	ENSP00000354635.4:p.Gln1501=
ENST00000361915.7:c.4552C=	ENSP00000355106.3:p.Gln1518=
ENST00000370161.6:c.4504C=	ENSP00000359180.2:p.Gln1502=
ENST00000370163.7:c.4552C=	ENSP00000359182.3:p.Gln1518=
ENST00000370165.7:c.4552C=	ENSP00000359184.3:p.Gln1518=
NM_000028.2:c.4552C=	NP_000019.2:p.Gln1518=
NM_000642.2:c.4552C=	NP_000633.2:p.Gln1518=
NM_000643.2:c.4552C=	NP_000634.2:p.Gln1518=
NM_000644.2:c.4552C=	NP_000635.2:p.Gln1518=
NM_000645.2:c.4501C=	NP_000636.2:p.Gln1501=
NM_000646.2:c.4504C=	NP_000637.2:p.Gln1502=
XM_005270557.1:c.4552C=	XP_005270614.1:p.Gln1518=
XR_947626.1:n.1317+2634G=
XR_947627.1:n.1206+2634G=
XR_947628.1:n.1311+2634G=
XR_947630.1:n.1249+2634G=
XR_947632.1:n.1135+2634G=
XR_947633.1:n.1246+2634G=
XR_947634.1:n.660+2634G=
XR_947635.1:n.728+2634G=
XM_005270557.2:c.4552C=	XP_005270614.1:p.Gln1518=
XM_017000501.2:c.2812C=	XP_016855990.1:p.Gln938=
NM_000642.3:c.4552C= MANE Select	NP_000633.2:p.Gln1518=