Canonical Allele Identifier: CA1183937264

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99900713_99900714delinsGA , CM000663.2:g.99900713_99900714delinsGA	GRCh38
NC_000001.10:g.100366269_100366270delinsGA , CM000663.1:g.100366269_100366270delinsGA	GRCh37
NC_000001.9:g.100138857_100138858delinsGA	NCBI36
NG_012865.1:g.55630_55631delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.3440_3441delinsGA MANE Select	ENSP00000355106.3:p.Arg1147=
ENST00000637337.1:n.3651_3652delinsGA
ENST00000294724.8:c.3440_3441delinsGA	ENSP00000294724.4:p.Arg1147=
ENST00000361302.7:c.3392_3393delinsGA	ENSP00000354971.3:p.Arg1131=
ENST00000361522.4:c.3389_3390delinsGA	ENSP00000354635.4:p.Arg1130=
ENST00000361915.7:c.3440_3441delinsGA	ENSP00000355106.3:p.Arg1147=
ENST00000370161.6:c.3392_3393delinsGA	ENSP00000359180.2:p.Arg1131=
ENST00000370163.7:c.3440_3441delinsGA	ENSP00000359182.3:p.Arg1147=
ENST00000370165.7:c.3440_3441delinsGA	ENSP00000359184.3:p.Arg1147=
NM_000028.2:c.3440_3441delinsGA	NP_000019.2:p.Arg1147=
NM_000642.2:c.3440_3441delinsGA	NP_000633.2:p.Arg1147=
NM_000643.2:c.3440_3441delinsGA	NP_000634.2:p.Arg1147=
NM_000644.2:c.3440_3441delinsGA	NP_000635.2:p.Arg1147=
NM_000645.2:c.3389_3390delinsGA	NP_000636.2:p.Arg1130=
NM_000646.2:c.3392_3393delinsGA	NP_000637.2:p.Arg1131=
XM_005270557.1:c.3440_3441delinsGA	XP_005270614.1:p.Arg1147=
XM_005270557.2:c.3440_3441delinsGA	XP_005270614.1:p.Arg1147=
XM_017000501.2:c.1700_1701delinsGA	XP_016855990.1:p.Arg567=
NM_000642.3:c.3440_3441delinsGA MANE Select	NP_000633.2:p.Arg1147=