Canonical Allele Identifier: CA1183928918

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99880397_99880400delinsCCCA , CM000663.2:g.99880397_99880400delinsCCCA	GRCh38
NC_000001.10:g.100345953_100345956delinsCCCA , CM000663.1:g.100345953_100345956delinsCCCA	GRCh37
NC_000001.9:g.100118541_100118544delinsCCCA	NCBI36
NG_012865.1:g.35314_35317delinsCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1736-235_1736-232delinsCCCA MANE Select	ENSP00000355106.3:n.1736-235_1736-232delinsCCCA
ENST00000637337.1:n.1947-235_1947-232delinsCCCA
ENST00000294724.8:c.1736-235_1736-232delinsCCCA	ENSP00000294724.4:n.1736-235_1736-232delinsCCCA
ENST00000361302.7:c.1688-235_1688-232delinsCCCA	ENSP00000354971.3:n.1688-235_1688-232delinsCCCA
ENST00000361522.4:c.1685-235_1685-232delinsCCCA	ENSP00000354635.4:n.1685-235_1685-232delinsCCCA
ENST00000361915.7:c.1736-235_1736-232delinsCCCA	ENSP00000355106.3:n.1736-235_1736-232delinsCCCA
ENST00000370161.6:c.1688-235_1688-232delinsCCCA	ENSP00000359180.2:n.1688-235_1688-232delinsCCCA
ENST00000370163.7:c.1736-235_1736-232delinsCCCA	ENSP00000359182.3:n.1736-235_1736-232delinsCCCA
ENST00000370165.7:c.1736-235_1736-232delinsCCCA	ENSP00000359184.3:n.1736-235_1736-232delinsCCCA
NM_000028.2:c.1736-235_1736-232delinsCCCA	NP_000019.2:n.1736-235_1736-232delinsCCCA
NM_000642.2:c.1736-235_1736-232delinsCCCA	NP_000633.2:n.1736-235_1736-232delinsCCCA
NM_000643.2:c.1736-235_1736-232delinsCCCA	NP_000634.2:n.1736-235_1736-232delinsCCCA
NM_000644.2:c.1736-235_1736-232delinsCCCA	NP_000635.2:n.1736-235_1736-232delinsCCCA
NM_000645.2:c.1685-235_1685-232delinsCCCA	NP_000636.2:n.1685-235_1685-232delinsCCCA
NM_000646.2:c.1688-235_1688-232delinsCCCA	NP_000637.2:n.1688-235_1688-232delinsCCCA
XM_005270557.1:c.1736-235_1736-232delinsCCCA	XP_005270614.1:n.1736-235_1736-232delinsCCCA
XM_005270557.2:c.1736-235_1736-232delinsCCCA	XP_005270614.1:n.1736-235_1736-232delinsCCCA
XM_017000501.2:c.-5-235_-5-232delinsCCCA	XP_016855990.1:n.-5-235_-5-232delinsCCCA
NM_000642.3:c.1736-235_1736-232delinsCCCA MANE Select	NP_000633.2:n.1736-235_1736-232delinsCCCA