Canonical Allele Identifier: CA2744755358

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99864641_99864642insCACCCCAAACACACCCA , CM000663.2:g.99864641_99864642insCACCCCAAACACACCCA	GRCh38
NC_000001.10:g.100330197_100330198insCACCCCAAACACACCCA , CM000663.1:g.100330197_100330198insCACCCCAAACACACCCA	GRCh37
NC_000001.9:g.100102785_100102786insCACCCCAAACACACCCA	NCBI36
NG_012865.1:g.19558_19559insCACCCCAAACACACCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.664+52_664+53insCACCCCAAACACACCCA MANE Select	ENSP00000355106.3:n.664+52_664+53insCACCCCAAACACACCCA
ENST00000637337.1:n.875+52_875+53insCACCCCAAACACACCCA
ENST00000294724.8:c.664+52_664+53insCACCCCAAACACACCCA	ENSP00000294724.4:n.664+52_664+53insCACCCCAAACACACCCA
ENST00000361302.7:c.616+52_616+53insCACCCCAAACACACCCA	ENSP00000354971.3:n.616+52_616+53insCACCCCAAACACACCCA
ENST00000361522.4:c.613+52_613+53insCACCCCAAACACACCCA	ENSP00000354635.4:n.613+52_613+53insCACCCCAAACACACCCA
ENST00000361915.7:c.664+52_664+53insCACCCCAAACACACCCA	ENSP00000355106.3:n.664+52_664+53insCACCCCAAACACACCCA
ENST00000370161.6:c.616+52_616+53insCACCCCAAACACACCCA	ENSP00000359180.2:n.616+52_616+53insCACCCCAAACACACCCA
ENST00000370163.7:c.664+52_664+53insCACCCCAAACACACCCA	ENSP00000359182.3:n.664+52_664+53insCACCCCAAACACACCCA
ENST00000370165.7:c.664+52_664+53insCACCCCAAACACACCCA	ENSP00000359184.3:n.664+52_664+53insCACCCCAAACACACCCA
NM_000028.2:c.664+52_664+53insCACCCCAAACACACCCA	NP_000019.2:n.664+52_664+53insCACCCCAAACACACCCA
NM_000642.2:c.664+52_664+53insCACCCCAAACACACCCA	NP_000633.2:n.664+52_664+53insCACCCCAAACACACCCA
NM_000643.2:c.664+52_664+53insCACCCCAAACACACCCA	NP_000634.2:n.664+52_664+53insCACCCCAAACACACCCA
NM_000644.2:c.664+52_664+53insCACCCCAAACACACCCA	NP_000635.2:n.664+52_664+53insCACCCCAAACACACCCA
NM_000645.2:c.613+52_613+53insCACCCCAAACACACCCA	NP_000636.2:n.613+52_613+53insCACCCCAAACACACCCA
NM_000646.2:c.616+52_616+53insCACCCCAAACACACCCA	NP_000637.2:n.616+52_616+53insCACCCCAAACACACCCA
XM_005270557.1:c.664+52_664+53insCACCCCAAACACACCCA	XP_005270614.1:n.664+52_664+53insCACCCCAAACACACCCA
XM_005270557.2:c.664+52_664+53insCACCCCAAACACACCCA	XP_005270614.1:n.664+52_664+53insCACCCCAAACACACCCA
NM_000642.3:c.664+52_664+53insCACCCCAAACACACCCA MANE Select	NP_000633.2:n.664+52_664+53insCACCCCAAACACACCCA