Canonical Allele Identifier: CA2574444200

Gene: AGL

Linked Data

• gnomAD v4: 1-99851117-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99851118del , CM000663.2:g.99851118del	GRCh38
NC_000001.10:g.100316674del , CM000663.1:g.100316674del	GRCh37
NC_000001.9:g.100089262del	NCBI36
NG_012865.1:g.6035del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.76del MANE Select	ENSP00000355106.3:p.Glu26AsnfsTer10
ENST00000294724.8:c.76del	ENSP00000294724.4:p.Glu26AsnfsTer10
ENST00000361302.7:c.-116del	ENSP00000354971.3:n.-116del
ENST00000361915.7:c.76del	ENSP00000355106.3:p.Glu26AsnfsTer10
ENST00000370163.7:c.76del	ENSP00000359182.3:p.Glu26AsnfsTer10
ENST00000370165.7:c.76del	ENSP00000359184.3:p.Glu26AsnfsTer10
NM_000028.2:c.76del	NP_000019.2:p.Glu26AsnfsTer10
NM_000642.2:c.76del	NP_000633.2:p.Glu26AsnfsTer10
NM_000643.2:c.76del	NP_000634.2:p.Glu26AsnfsTer10
NM_000644.2:c.76del	NP_000635.2:p.Glu26AsnfsTer10
NM_000646.2:c.-116del	NP_000637.2:n.-116del
XM_005270557.1:c.76del	XP_005270614.1:p.Glu26AsnfsTer10
XM_005270557.2:c.76del	XP_005270614.1:p.Glu26AsnfsTer10
NM_000642.3:c.76del MANE Select	NP_000633.2:p.Glu26AsnfsTer10