Canonical Allele Identifier: CA1183924524

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99862399_99862400delinsAG , CM000663.2:g.99862399_99862400delinsAG	GRCh38
NC_000001.10:g.100327955_100327956delinsAG , CM000663.1:g.100327955_100327956delinsAG	GRCh37
NC_000001.9:g.100100543_100100544delinsAG	NCBI36
NG_012865.1:g.17316_17317delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.436_437delinsAG MANE Select	ENSP00000355106.3:p.Arg146=
ENST00000637337.1:n.647_648delinsAG
ENST00000294724.8:c.436_437delinsAG	ENSP00000294724.4:p.Arg146=
ENST00000361302.7:c.388_389delinsAG	ENSP00000354971.3:p.Arg130=
ENST00000361522.4:c.385_386delinsAG	ENSP00000354635.4:p.Arg129=
ENST00000361915.7:c.436_437delinsAG	ENSP00000355106.3:p.Arg146=
ENST00000370161.6:c.388_389delinsAG	ENSP00000359180.2:p.Arg130=
ENST00000370163.7:c.436_437delinsAG	ENSP00000359182.3:p.Arg146=
ENST00000370165.7:c.436_437delinsAG	ENSP00000359184.3:p.Arg146=
NM_000028.2:c.436_437delinsAG	NP_000019.2:p.Arg146=
NM_000642.2:c.436_437delinsAG	NP_000633.2:p.Arg146=
NM_000643.2:c.436_437delinsAG	NP_000634.2:p.Arg146=
NM_000644.2:c.436_437delinsAG	NP_000635.2:p.Arg146=
NM_000645.2:c.385_386delinsAG	NP_000636.2:p.Arg129=
NM_000646.2:c.388_389delinsAG	NP_000637.2:p.Arg130=
XM_005270557.1:c.436_437delinsAG	XP_005270614.1:p.Arg146=
XM_005270557.2:c.436_437delinsAG	XP_005270614.1:p.Arg146=
NM_000642.3:c.436_437delinsAG MANE Select	NP_000633.2:p.Arg146=