Canonical Allele Identifier: CA1183945108

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921790G= , CM000663.2:g.99921790G=	GRCh38
NC_000001.10:g.100387346G= , CM000663.1:g.100387346G=	GRCh37
NC_000001.9:g.100159934G=	NCBI36
NG_012865.1:g.76707G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.*139G= MANE Select	ENSP00000355106.3:n.*139G=
ENST00000637337.1:n.4949G=
ENST00000294724.8:c.*139G=	ENSP00000294724.4:n.*139G=
ENST00000361302.7:c.*139G=	ENSP00000354971.3:n.*139G=
ENST00000361522.4:c.*139G=	ENSP00000354635.4:n.*139G=
ENST00000361915.7:c.*139G=	ENSP00000355106.3:n.*139G=
ENST00000370161.6:c.4690G=	ENSP00000359180.2:n.4690G=
ENST00000370163.7:c.*139G=	ENSP00000359182.3:n.*139G=
ENST00000370165.7:c.*139G=	ENSP00000359184.3:n.*139G=
NM_000028.2:c.*139G=	NP_000019.2:n.*139G=
NM_000642.2:c.*139G=	NP_000633.2:n.*139G=
NM_000643.2:c.*139G=	NP_000634.2:n.*139G=
NM_000644.2:c.*139G=	NP_000635.2:n.*139G=
NM_000645.2:c.*139G=	NP_000636.2:n.*139G=
NM_000646.2:c.*139G=	NP_000637.2:n.*139G=
XM_005270557.1:c.*139G=	XP_005270614.1:n.*139G=
XR_947626.1:n.1317+2448C=
XR_947627.1:n.1206+2448C=
XR_947628.1:n.1311+2448C=
XR_947630.1:n.1249+2448C=
XR_947632.1:n.1135+2448C=
XR_947633.1:n.1246+2448C=
XR_947634.1:n.660+2448C=
XR_947635.1:n.728+2448C=
XM_005270557.2:c.*139G=	XP_005270614.1:n.*139G=
XM_017000501.2:c.*139G=	XP_016855990.1:n.*139G=
NM_000642.3:c.*139G= MANE Select	NP_000633.2:n.*139G=