Canonical Allele Identifier: CA1183924502

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99862382_99862385delinsTTGA , CM000663.2:g.99862382_99862385delinsTTGA	GRCh38
NC_000001.10:g.100327938_100327941delinsTTGA , CM000663.1:g.100327938_100327941delinsTTGA	GRCh37
NC_000001.9:g.100100526_100100529delinsTTGA	NCBI36
NG_012865.1:g.17299_17302delinsTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.419_422delinsTTGA MANE Select	ENSP00000355106.3:p.Phe140=
ENST00000637337.1:n.630_633delinsTTGA
ENST00000294724.8:c.419_422delinsTTGA	ENSP00000294724.4:p.Phe140=
ENST00000361302.7:c.371_374delinsTTGA	ENSP00000354971.3:p.Phe124=
ENST00000361522.4:c.368_371delinsTTGA	ENSP00000354635.4:p.Phe123=
ENST00000361915.7:c.419_422delinsTTGA	ENSP00000355106.3:p.Phe140=
ENST00000370161.6:c.371_374delinsTTGA	ENSP00000359180.2:p.Phe124=
ENST00000370163.7:c.419_422delinsTTGA	ENSP00000359182.3:p.Phe140=
ENST00000370165.7:c.419_422delinsTTGA	ENSP00000359184.3:p.Phe140=
NM_000028.2:c.419_422delinsTTGA	NP_000019.2:p.Phe140=
NM_000642.2:c.419_422delinsTTGA	NP_000633.2:p.Phe140=
NM_000643.2:c.419_422delinsTTGA	NP_000634.2:p.Phe140=
NM_000644.2:c.419_422delinsTTGA	NP_000635.2:p.Phe140=
NM_000645.2:c.368_371delinsTTGA	NP_000636.2:p.Phe123=
NM_000646.2:c.371_374delinsTTGA	NP_000637.2:p.Phe124=
XM_005270557.1:c.419_422delinsTTGA	XP_005270614.1:p.Phe140=
XM_005270557.2:c.419_422delinsTTGA	XP_005270614.1:p.Phe140=
NM_000642.3:c.419_422delinsTTGA MANE Select	NP_000633.2:p.Phe140=