Canonical Allele Identifier: CA2646738767

Gene: AGL

Linked Data

• gnomAD v4: 1-99910938-TTTACA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99910942_99910946del , CM000663.2:g.99910942_99910946del	GRCh38
NC_000001.10:g.100376498_100376502del , CM000663.1:g.100376498_100376502del	GRCh37
NC_000001.9:g.100149086_100149090del	NCBI36
NG_012865.1:g.65859_65863del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.3836+95_3836+99del MANE Select	ENSP00000355106.3:n.3836+95_3836+99del
ENST00000637337.1:n.4047+95_4047+99del
ENST00000294724.8:c.3836+95_3836+99del	ENSP00000294724.4:n.3836+95_3836+99del
ENST00000361302.7:c.3788+95_3788+99del	ENSP00000354971.3:n.3788+95_3788+99del
ENST00000361522.4:c.3785+95_3785+99del	ENSP00000354635.4:n.3785+95_3785+99del
ENST00000361915.7:c.3836+95_3836+99del	ENSP00000355106.3:n.3836+95_3836+99del
ENST00000370161.6:c.3788+95_3788+99del	ENSP00000359180.2:n.3788+95_3788+99del
ENST00000370163.7:c.3836+95_3836+99del	ENSP00000359182.3:n.3836+95_3836+99del
ENST00000370165.7:c.3836+95_3836+99del	ENSP00000359184.3:n.3836+95_3836+99del
NM_000028.2:c.3836+95_3836+99del	NP_000019.2:n.3836+95_3836+99del
NM_000642.2:c.3836+95_3836+99del	NP_000633.2:n.3836+95_3836+99del
NM_000643.2:c.3836+95_3836+99del	NP_000634.2:n.3836+95_3836+99del
NM_000644.2:c.3836+95_3836+99del	NP_000635.2:n.3836+95_3836+99del
NM_000645.2:c.3785+95_3785+99del	NP_000636.2:n.3785+95_3785+99del
NM_000646.2:c.3788+95_3788+99del	NP_000637.2:n.3788+95_3788+99del
XM_005270557.1:c.3836+95_3836+99del	XP_005270614.1:n.3836+95_3836+99del
XM_005270557.2:c.3836+95_3836+99del	XP_005270614.1:n.3836+95_3836+99del
XM_017000501.2:c.2096+95_2096+99del	XP_016855990.1:n.2096+95_2096+99del
NM_000642.3:c.3836+95_3836+99del MANE Select	NP_000633.2:n.3836+95_3836+99del