Canonical Allele Identifier: CA1183926785

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99875249_99875250delinsAG , CM000663.2:g.99875249_99875250delinsAG	GRCh38
NC_000001.10:g.100340805_100340806delinsAG , CM000663.1:g.100340805_100340806delinsAG	GRCh37
NC_000001.9:g.100113393_100113394delinsAG	NCBI36
NG_012865.1:g.30166_30167delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1178_1179delinsAG MANE Select	ENSP00000355106.3:p.Gln393=
ENST00000637337.1:n.1389_1390delinsAG
ENST00000294724.8:c.1178_1179delinsAG	ENSP00000294724.4:p.Gln393=
ENST00000361302.7:c.1130_1131delinsAG	ENSP00000354971.3:p.Gln377=
ENST00000361522.4:c.1127_1128delinsAG	ENSP00000354635.4:p.Gln376=
ENST00000361915.7:c.1178_1179delinsAG	ENSP00000355106.3:p.Gln393=
ENST00000370161.6:c.1130_1131delinsAG	ENSP00000359180.2:p.Gln377=
ENST00000370163.7:c.1178_1179delinsAG	ENSP00000359182.3:p.Gln393=
ENST00000370165.7:c.1178_1179delinsAG	ENSP00000359184.3:p.Gln393=
ENST00000477753.1:n.437_438delinsAG
NM_000028.2:c.1178_1179delinsAG	NP_000019.2:p.Gln393=
NM_000642.2:c.1178_1179delinsAG	NP_000633.2:p.Gln393=
NM_000643.2:c.1178_1179delinsAG	NP_000634.2:p.Gln393=
NM_000644.2:c.1178_1179delinsAG	NP_000635.2:p.Gln393=
NM_000645.2:c.1127_1128delinsAG	NP_000636.2:p.Gln376=
NM_000646.2:c.1130_1131delinsAG	NP_000637.2:p.Gln377=
XM_005270557.1:c.1178_1179delinsAG	XP_005270614.1:p.Gln393=
XM_005270557.2:c.1178_1179delinsAG	XP_005270614.1:p.Gln393=
NM_000642.3:c.1178_1179delinsAG MANE Select	NP_000633.2:p.Gln393=