Canonical Allele Identifier: CA2646736976

Gene: AGL

Linked Data

• gnomAD v4: 1-99875294-C-CTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99875296_99875297insTTTTT , CM000663.2:g.99875296_99875297insTTTTT	GRCh38
NC_000001.10:g.100340852_100340853insTTTTT , CM000663.1:g.100340852_100340853insTTTTT	GRCh37
NC_000001.9:g.100113440_100113441insTTTTT	NCBI36
NG_012865.1:g.30213_30214insTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1185+40_1185+41insTTTTT MANE Select	ENSP00000355106.3:n.1185+40_1185+41insTTTTT
ENST00000637337.1:n.1396+40_1396+41insTTTTT
ENST00000294724.8:c.1185+40_1185+41insTTTTT	ENSP00000294724.4:n.1185+40_1185+41insTTTTT
ENST00000361302.7:c.1137+40_1137+41insTTTTT	ENSP00000354971.3:n.1137+40_1137+41insTTTTT
ENST00000361522.4:c.1134+40_1134+41insTTTTT	ENSP00000354635.4:n.1134+40_1134+41insTTTTT
ENST00000361915.7:c.1185+40_1185+41insTTTTT	ENSP00000355106.3:n.1185+40_1185+41insTTTTT
ENST00000370161.6:c.1137+40_1137+41insTTTTT	ENSP00000359180.2:n.1137+40_1137+41insTTTTT
ENST00000370163.7:c.1185+40_1185+41insTTTTT	ENSP00000359182.3:n.1185+40_1185+41insTTTTT
ENST00000370165.7:c.1185+40_1185+41insTTTTT	ENSP00000359184.3:n.1185+40_1185+41insTTTTT
ENST00000477753.1:n.444+40_444+41insTTTTT
NM_000028.2:c.1185+40_1185+41insTTTTT	NP_000019.2:n.1185+40_1185+41insTTTTT
NM_000642.2:c.1185+40_1185+41insTTTTT	NP_000633.2:n.1185+40_1185+41insTTTTT
NM_000643.2:c.1185+40_1185+41insTTTTT	NP_000634.2:n.1185+40_1185+41insTTTTT
NM_000644.2:c.1185+40_1185+41insTTTTT	NP_000635.2:n.1185+40_1185+41insTTTTT
NM_000645.2:c.1134+40_1134+41insTTTTT	NP_000636.2:n.1134+40_1134+41insTTTTT
NM_000646.2:c.1137+40_1137+41insTTTTT	NP_000637.2:n.1137+40_1137+41insTTTTT
XM_005270557.1:c.1185+40_1185+41insTTTTT	XP_005270614.1:n.1185+40_1185+41insTTTTT
XM_005270557.2:c.1185+40_1185+41insTTTTT	XP_005270614.1:n.1185+40_1185+41insTTTTT
NM_000642.3:c.1185+40_1185+41insTTTTT MANE Select	NP_000633.2:n.1185+40_1185+41insTTTTT