Canonical Allele Identifier: CA2646734182

Gene: AGL

Linked Data

• gnomAD v4: 1-99870312-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99870312T>A , CM000663.2:g.99870312T>A	GRCh38
NC_000001.10:g.100335868T>A , CM000663.1:g.100335868T>A	GRCh37
NC_000001.9:g.100108456T>A	NCBI36
NG_012865.1:g.25229T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.665-88T>A MANE Select	ENSP00000355106.3:n.665-88T>A
ENST00000637337.1:n.876-88T>A
ENST00000294724.8:c.665-88T>A	ENSP00000294724.4:n.665-88T>A
ENST00000361302.7:c.617-88T>A	ENSP00000354971.3:n.617-88T>A
ENST00000361522.4:c.614-88T>A	ENSP00000354635.4:n.614-88T>A
ENST00000361915.7:c.665-88T>A	ENSP00000355106.3:n.665-88T>A
ENST00000370161.6:c.617-88T>A	ENSP00000359180.2:n.617-88T>A
ENST00000370163.7:c.665-88T>A	ENSP00000359182.3:n.665-88T>A
ENST00000370165.7:c.665-88T>A	ENSP00000359184.3:n.665-88T>A
NM_000028.2:c.665-88T>A	NP_000019.2:n.665-88T>A
NM_000642.2:c.665-88T>A	NP_000633.2:n.665-88T>A
NM_000643.2:c.665-88T>A	NP_000634.2:n.665-88T>A
NM_000644.2:c.665-88T>A	NP_000635.2:n.665-88T>A
NM_000645.2:c.614-88T>A	NP_000636.2:n.614-88T>A
NM_000646.2:c.617-88T>A	NP_000637.2:n.617-88T>A
XM_005270557.1:c.665-88T>A	XP_005270614.1:n.665-88T>A
XM_005270557.2:c.665-88T>A	XP_005270614.1:n.665-88T>A
NM_000642.3:c.665-88T>A MANE Select	NP_000633.2:n.665-88T>A