Canonical Allele Identifier: CA1183941678

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99916689T= , CM000663.2:g.99916689T=	GRCh38
NC_000001.10:g.100382245T= , CM000663.1:g.100382245T=	GRCh37
NC_000001.9:g.100154833T=	NCBI36
NG_012865.1:g.71606T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4439T= MANE Select	ENSP00000355106.3:p.Leu1480=
ENST00000637337.1:n.4650T=
ENST00000294724.8:c.4439T=	ENSP00000294724.4:p.Leu1480=
ENST00000361302.7:c.4391T=	ENSP00000354971.3:p.Leu1464=
ENST00000361522.4:c.4388T=	ENSP00000354635.4:p.Leu1463=
ENST00000361915.7:c.4439T=	ENSP00000355106.3:p.Leu1480=
ENST00000370161.6:c.4391T=	ENSP00000359180.2:p.Leu1464=
ENST00000370163.7:c.4439T=	ENSP00000359182.3:p.Leu1480=
ENST00000370165.7:c.4439T=	ENSP00000359184.3:p.Leu1480=
NM_000028.2:c.4439T=	NP_000019.2:p.Leu1480=
NM_000642.2:c.4439T=	NP_000633.2:p.Leu1480=
NM_000643.2:c.4439T=	NP_000634.2:p.Leu1480=
NM_000644.2:c.4439T=	NP_000635.2:p.Leu1480=
NM_000645.2:c.4388T=	NP_000636.2:p.Leu1463=
NM_000646.2:c.4391T=	NP_000637.2:p.Leu1464=
XM_005270557.1:c.4439T=	XP_005270614.1:p.Leu1480=
XR_947626.1:n.1318-3472A=
XR_947627.1:n.1207-3472A=
XR_947628.1:n.1312-3472A=
XR_947630.1:n.1250-3472A=
XR_947632.1:n.1136-3472A=
XR_947633.1:n.1247-3472A=
XR_947634.1:n.661-3472A=
XR_947635.1:n.729-3472A=
XM_005270557.2:c.4439T=	XP_005270614.1:p.Leu1480=
XM_017000501.2:c.2699T=	XP_016855990.1:p.Leu900=
NM_000642.3:c.4439T= MANE Select	NP_000633.2:p.Leu1480=