Canonical Allele Identifier: CA2695198098

Gene: AGL

Linked Data

• ClinVar Variation Id: 2680976
• ClinVar RCV Id: RCV003475769

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99870544dup , CM000663.2:g.99870544dup	GRCh38
NC_000001.10:g.100336100dup , CM000663.1:g.100336100dup	GRCh37
NC_000001.9:g.100108688dup	NCBI36
NG_012865.1:g.25461dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.809dup MANE Select	ENSP00000355106.3:p.Ile271AsnfsTer6
ENST00000637337.1:n.1020dup
ENST00000294724.8:c.809dup	ENSP00000294724.4:p.Ile271AsnfsTer6
ENST00000361302.7:c.761dup	ENSP00000354971.3:p.Ile255AsnfsTer6
ENST00000361522.4:c.758dup	ENSP00000354635.4:p.Ile254AsnfsTer6
ENST00000361915.7:c.809dup	ENSP00000355106.3:p.Ile271AsnfsTer6
ENST00000370161.6:c.761dup	ENSP00000359180.2:p.Ile255AsnfsTer6
ENST00000370163.7:c.809dup	ENSP00000359182.3:p.Ile271AsnfsTer6
ENST00000370165.7:c.809dup	ENSP00000359184.3:p.Ile271AsnfsTer6
NM_000028.2:c.809dup	NP_000019.2:p.Ile271AsnfsTer6
NM_000642.2:c.809dup	NP_000633.2:p.Ile271AsnfsTer6
NM_000643.2:c.809dup	NP_000634.2:p.Ile271AsnfsTer6
NM_000644.2:c.809dup	NP_000635.2:p.Ile271AsnfsTer6
NM_000645.2:c.758dup	NP_000636.2:p.Ile254AsnfsTer6
NM_000646.2:c.761dup	NP_000637.2:p.Ile255AsnfsTer6
XM_005270557.1:c.809dup	XP_005270614.1:p.Ile271AsnfsTer6
XM_005270557.2:c.809dup	XP_005270614.1:p.Ile271AsnfsTer6
NM_000642.3:c.809dup MANE Select	NP_000633.2:p.Ile271AsnfsTer6