Canonical Allele Identifier: CA2550303278

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99881247_99881248insTT , CM000663.2:g.99881247_99881248insTT	GRCh38
NC_000001.10:g.100346803_100346804insTT , CM000663.1:g.100346803_100346804insTT	GRCh37
NC_000001.9:g.100119391_100119392insTT	NCBI36
NG_012865.1:g.36164_36165insTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.2002-45_2002-44insTT MANE Select	ENSP00000355106.3:n.2002-45_2002-44insTT
ENST00000637337.1:n.2213-45_2213-44insTT
ENST00000294724.8:c.2002-45_2002-44insTT	ENSP00000294724.4:n.2002-45_2002-44insTT
ENST00000361302.7:c.1954-45_1954-44insTT	ENSP00000354971.3:n.1954-45_1954-44insTT
ENST00000361522.4:c.1951-45_1951-44insTT	ENSP00000354635.4:n.1951-45_1951-44insTT
ENST00000361915.7:c.2002-45_2002-44insTT	ENSP00000355106.3:n.2002-45_2002-44insTT
ENST00000370161.6:c.1954-45_1954-44insTT	ENSP00000359180.2:n.1954-45_1954-44insTT
ENST00000370163.7:c.2002-45_2002-44insTT	ENSP00000359182.3:n.2002-45_2002-44insTT
ENST00000370165.7:c.2002-45_2002-44insTT	ENSP00000359184.3:n.2002-45_2002-44insTT
NM_000028.2:c.2002-45_2002-44insTT	NP_000019.2:n.2002-45_2002-44insTT
NM_000642.2:c.2002-45_2002-44insTT	NP_000633.2:n.2002-45_2002-44insTT
NM_000643.2:c.2002-45_2002-44insTT	NP_000634.2:n.2002-45_2002-44insTT
NM_000644.2:c.2002-45_2002-44insTT	NP_000635.2:n.2002-45_2002-44insTT
NM_000645.2:c.1951-45_1951-44insTT	NP_000636.2:n.1951-45_1951-44insTT
NM_000646.2:c.1954-45_1954-44insTT	NP_000637.2:n.1954-45_1954-44insTT
XM_005270557.1:c.2002-45_2002-44insTT	XP_005270614.1:n.2002-45_2002-44insTT
XM_005270557.2:c.2002-45_2002-44insTT	XP_005270614.1:n.2002-45_2002-44insTT
XM_017000501.2:c.262-45_262-44insTT	XP_016855990.1:n.262-45_262-44insTT
NM_000642.3:c.2002-45_2002-44insTT MANE Select	NP_000633.2:n.2002-45_2002-44insTT