Canonical Allele Identifier: CA1183924493

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99862379_99862380delinsCT , CM000663.2:g.99862379_99862380delinsCT	GRCh38
NC_000001.10:g.100327935_100327936delinsCT , CM000663.1:g.100327935_100327936delinsCT	GRCh37
NC_000001.9:g.100100523_100100524delinsCT	NCBI36
NG_012865.1:g.17296_17297delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.416_417delinsCT MANE Select	ENSP00000355106.3:p.Pro139=
ENST00000637337.1:n.627_628delinsCT
ENST00000294724.8:c.416_417delinsCT	ENSP00000294724.4:p.Pro139=
ENST00000361302.7:c.368_369delinsCT	ENSP00000354971.3:p.Pro123=
ENST00000361522.4:c.365_366delinsCT	ENSP00000354635.4:p.Pro122=
ENST00000361915.7:c.416_417delinsCT	ENSP00000355106.3:p.Pro139=
ENST00000370161.6:c.368_369delinsCT	ENSP00000359180.2:p.Pro123=
ENST00000370163.7:c.416_417delinsCT	ENSP00000359182.3:p.Pro139=
ENST00000370165.7:c.416_417delinsCT	ENSP00000359184.3:p.Pro139=
NM_000028.2:c.416_417delinsCT	NP_000019.2:p.Pro139=
NM_000642.2:c.416_417delinsCT	NP_000633.2:p.Pro139=
NM_000643.2:c.416_417delinsCT	NP_000634.2:p.Pro139=
NM_000644.2:c.416_417delinsCT	NP_000635.2:p.Pro139=
NM_000645.2:c.365_366delinsCT	NP_000636.2:p.Pro122=
NM_000646.2:c.368_369delinsCT	NP_000637.2:p.Pro123=
XM_005270557.1:c.416_417delinsCT	XP_005270614.1:p.Pro139=
XM_005270557.2:c.416_417delinsCT	XP_005270614.1:p.Pro139=
NM_000642.3:c.416_417delinsCT MANE Select	NP_000633.2:p.Pro139=