Canonical Allele Identifier: CA965996

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99851078_99851079insCG , CM000663.2:g.99851078_99851079insCG	GRCh38
NC_000001.10:g.100316634_100316635insCG , CM000663.1:g.100316634_100316635insCG	GRCh37
NC_000001.9:g.100089222_100089223insCG	NCBI36
NG_012865.1:g.5995_5996insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.36_37insCG MANE Select	ENSP00000355106.3:p.Asn13ArgfsTer24
ENST00000294724.8:c.36_37insCG	ENSP00000294724.4:p.Asn13ArgfsTer24
ENST00000361302.7:c.-156_-155insCG	ENSP00000354971.3:n.-156_-155insCG
ENST00000361915.7:c.36_37insCG	ENSP00000355106.3:p.Asn13ArgfsTer24
ENST00000370163.7:c.36_37insCG	ENSP00000359182.3:p.Asn13ArgfsTer24
ENST00000370165.7:c.36_37insCG	ENSP00000359184.3:p.Asn13ArgfsTer24
NM_000028.2:c.36_37insCG	NP_000019.2:p.Asn13ArgfsTer24
NM_000642.2:c.36_37insCG	NP_000633.2:p.Asn13ArgfsTer24
NM_000643.2:c.36_37insCG	NP_000634.2:p.Asn13ArgfsTer24
NM_000644.2:c.36_37insCG	NP_000635.2:p.Asn13ArgfsTer24
NM_000646.2:c.-156_-155insCG	NP_000637.2:n.-156_-155insCG
XM_005270557.1:c.36_37insCG	XP_005270614.1:p.Asn13ArgfsTer24
XM_005270557.2:c.36_37insCG	XP_005270614.1:p.Asn13ArgfsTer24
NM_000642.3:c.36_37insCG MANE Select	NP_000633.2:p.Asn13ArgfsTer24