Canonical Allele Identifier: CA2646737000

Gene: AGL

Linked Data

• gnomAD v4: 1-99875342-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99875345dup , CM000663.2:g.99875345dup	GRCh38
NC_000001.10:g.100340901dup , CM000663.1:g.100340901dup	GRCh37
NC_000001.9:g.100113489dup	NCBI36
NG_012865.1:g.30262dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1186-13dup MANE Select	ENSP00000355106.3:n.1186-13dup
ENST00000637337.1:n.1397-13dup
ENST00000294724.8:c.1186-13dup	ENSP00000294724.4:n.1186-13dup
ENST00000361302.7:c.1138-13dup	ENSP00000354971.3:n.1138-13dup
ENST00000361522.4:c.1135-13dup	ENSP00000354635.4:n.1135-13dup
ENST00000361915.7:c.1186-13dup	ENSP00000355106.3:n.1186-13dup
ENST00000370161.6:c.1138-13dup	ENSP00000359180.2:n.1138-13dup
ENST00000370163.7:c.1186-13dup	ENSP00000359182.3:n.1186-13dup
ENST00000370165.7:c.1186-13dup	ENSP00000359184.3:n.1186-13dup
ENST00000477753.1:n.445-13dup
NM_000028.2:c.1186-13dup	NP_000019.2:n.1186-13dup
NM_000642.2:c.1186-13dup	NP_000633.2:n.1186-13dup
NM_000643.2:c.1186-13dup	NP_000634.2:n.1186-13dup
NM_000644.2:c.1186-13dup	NP_000635.2:n.1186-13dup
NM_000645.2:c.1135-13dup	NP_000636.2:n.1135-13dup
NM_000646.2:c.1138-13dup	NP_000637.2:n.1138-13dup
XM_005270557.1:c.1186-13dup	XP_005270614.1:n.1186-13dup
XM_005270557.2:c.1186-13dup	XP_005270614.1:n.1186-13dup
NM_000642.3:c.1186-13dup MANE Select	NP_000633.2:n.1186-13dup