Canonical Allele Identifier: CA1183945154

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921850T= , CM000663.2:g.99921850T=	GRCh38
NC_000001.10:g.100387406T= , CM000663.1:g.100387406T=	GRCh37
NC_000001.9:g.100159994T=	NCBI36
NG_012865.1:g.76767T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.*199T= MANE Select	ENSP00000355106.3:n.*199T=
ENST00000637337.1:n.5009T=
ENST00000294724.8:c.*199T=	ENSP00000294724.4:n.*199T=
ENST00000361302.7:c.*199T=	ENSP00000354971.3:n.*199T=
ENST00000361522.4:c.*199T=	ENSP00000354635.4:n.*199T=
ENST00000361915.7:c.*199T=	ENSP00000355106.3:n.*199T=
ENST00000370161.6:c.4750T=	ENSP00000359180.2:n.4750T=
ENST00000370163.7:c.*199T=	ENSP00000359182.3:n.*199T=
ENST00000370165.7:c.*199T=	ENSP00000359184.3:n.*199T=
NM_000028.2:c.*199T=	NP_000019.2:n.*199T=
NM_000642.2:c.*199T=	NP_000633.2:n.*199T=
NM_000643.2:c.*199T=	NP_000634.2:n.*199T=
NM_000644.2:c.*199T=	NP_000635.2:n.*199T=
NM_000645.2:c.*199T=	NP_000636.2:n.*199T=
NM_000646.2:c.*199T=	NP_000637.2:n.*199T=
XM_005270557.1:c.*199T=	XP_005270614.1:n.*199T=
XR_947626.1:n.1317+2388A=
XR_947627.1:n.1206+2388A=
XR_947628.1:n.1311+2388A=
XR_947630.1:n.1249+2388A=
XR_947632.1:n.1135+2388A=
XR_947633.1:n.1246+2388A=
XR_947634.1:n.660+2388A=
XR_947635.1:n.728+2388A=
XM_005270557.2:c.*199T=	XP_005270614.1:n.*199T=
XM_017000501.2:c.*199T=	XP_016855990.1:n.*199T=
NM_000642.3:c.*199T= MANE Select	NP_000633.2:n.*199T=