Canonical Allele Identifier: CA1183926685

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99874978_99874979delinsTG , CM000663.2:g.99874978_99874979delinsTG	GRCh38
NC_000001.10:g.100340534_100340535delinsTG , CM000663.1:g.100340534_100340535delinsTG	GRCh37
NC_000001.9:g.100113122_100113123delinsTG	NCBI36
NG_012865.1:g.29895_29896delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1082+168_1082+169delinsTG MANE Select	ENSP00000355106.3:n.1082+168_1082+169delinsTG
ENST00000637337.1:n.1293+168_1293+169delinsTG
ENST00000294724.8:c.1082+168_1082+169delinsTG	ENSP00000294724.4:n.1082+168_1082+169delinsTG
ENST00000361302.7:c.1034+168_1034+169delinsTG	ENSP00000354971.3:n.1034+168_1034+169delinsTG
ENST00000361522.4:c.1031+168_1031+169delinsTG	ENSP00000354635.4:n.1031+168_1031+169delinsTG
ENST00000361915.7:c.1082+168_1082+169delinsTG	ENSP00000355106.3:n.1082+168_1082+169delinsTG
ENST00000370161.6:c.1034+168_1034+169delinsTG	ENSP00000359180.2:n.1034+168_1034+169delinsTG
ENST00000370163.7:c.1082+168_1082+169delinsTG	ENSP00000359182.3:n.1082+168_1082+169delinsTG
ENST00000370165.7:c.1082+168_1082+169delinsTG	ENSP00000359184.3:n.1082+168_1082+169delinsTG
ENST00000477753.1:n.341+168_341+169delinsTG
NM_000028.2:c.1082+168_1082+169delinsTG	NP_000019.2:n.1082+168_1082+169delinsTG
NM_000642.2:c.1082+168_1082+169delinsTG	NP_000633.2:n.1082+168_1082+169delinsTG
NM_000643.2:c.1082+168_1082+169delinsTG	NP_000634.2:n.1082+168_1082+169delinsTG
NM_000644.2:c.1082+168_1082+169delinsTG	NP_000635.2:n.1082+168_1082+169delinsTG
NM_000645.2:c.1031+168_1031+169delinsTG	NP_000636.2:n.1031+168_1031+169delinsTG
NM_000646.2:c.1034+168_1034+169delinsTG	NP_000637.2:n.1034+168_1034+169delinsTG
XM_005270557.1:c.1082+168_1082+169delinsTG	XP_005270614.1:n.1082+168_1082+169delinsTG
XM_005270557.2:c.1082+168_1082+169delinsTG	XP_005270614.1:n.1082+168_1082+169delinsTG
NM_000642.3:c.1082+168_1082+169delinsTG MANE Select	NP_000633.2:n.1082+168_1082+169delinsTG