Canonical Allele Identifier: CA2646738733

Gene: AGL

Linked Data

• gnomAD v4: 1-99910906-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99910906G>A , CM000663.2:g.99910906G>A	GRCh38
NC_000001.10:g.100376462G>A , CM000663.1:g.100376462G>A	GRCh37
NC_000001.9:g.100149050G>A	NCBI36
NG_012865.1:g.65823G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.3836+59G>A MANE Select	ENSP00000355106.3:n.3836+59G>A
ENST00000637337.1:n.4047+59G>A
ENST00000294724.8:c.3836+59G>A	ENSP00000294724.4:n.3836+59G>A
ENST00000361302.7:c.3788+59G>A	ENSP00000354971.3:n.3788+59G>A
ENST00000361522.4:c.3785+59G>A	ENSP00000354635.4:n.3785+59G>A
ENST00000361915.7:c.3836+59G>A	ENSP00000355106.3:n.3836+59G>A
ENST00000370161.6:c.3788+59G>A	ENSP00000359180.2:n.3788+59G>A
ENST00000370163.7:c.3836+59G>A	ENSP00000359182.3:n.3836+59G>A
ENST00000370165.7:c.3836+59G>A	ENSP00000359184.3:n.3836+59G>A
NM_000028.2:c.3836+59G>A	NP_000019.2:n.3836+59G>A
NM_000642.2:c.3836+59G>A	NP_000633.2:n.3836+59G>A
NM_000643.2:c.3836+59G>A	NP_000634.2:n.3836+59G>A
NM_000644.2:c.3836+59G>A	NP_000635.2:n.3836+59G>A
NM_000645.2:c.3785+59G>A	NP_000636.2:n.3785+59G>A
NM_000646.2:c.3788+59G>A	NP_000637.2:n.3788+59G>A
XM_005270557.1:c.3836+59G>A	XP_005270614.1:n.3836+59G>A
XM_005270557.2:c.3836+59G>A	XP_005270614.1:n.3836+59G>A
XM_017000501.2:c.2096+59G>A	XP_016855990.1:n.2096+59G>A
NM_000642.3:c.3836+59G>A MANE Select	NP_000633.2:n.3836+59G>A