Canonical Allele Identifier: CA1183944800

Gene: AGL

Linked Data

• dbSNP Id: rs1655506154
• gnomAD v4: 1-99921494-T-TAAACTA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921494_99921495insAAACTA , CM000663.2:g.99921494_99921495insAAACTA	GRCh38
NC_000001.10:g.100387050_100387051insAAACTA , CM000663.1:g.100387050_100387051insAAACTA	GRCh37
NC_000001.9:g.100159638_100159639insAAACTA	NCBI36
NG_012865.1:g.76411_76412insAAACTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.4482-40_4482-39insAAACTA MANE Select	ENSP00000355106.3:n.4482-40_4482-39insAAA...
ENST00000637337.1:n.4693-40_4693-39insAAACTA
ENST00000294724.8:c.4482-40_4482-39insAAACTA	ENSP00000294724.4:n.4482-40_4482-39insAAA...
ENST00000361302.7:c.4434-40_4434-39insAAACTA	ENSP00000354971.3:n.4434-40_4434-39insAAA...
ENST00000361522.4:c.4431-40_4431-39insAAACTA	ENSP00000354635.4:n.4431-40_4431-39insAAA...
ENST00000361915.7:c.4482-40_4482-39insAAACTA	ENSP00000355106.3:n.4482-40_4482-39insAAA...
ENST00000370161.6:c.4434-40_4434-39insAAACTA	ENSP00000359180.2:n.4434-40_4434-39insAAA...
ENST00000370163.7:c.4482-40_4482-39insAAACTA	ENSP00000359182.3:n.4482-40_4482-39insAAA...
ENST00000370165.7:c.4482-40_4482-39insAAACTA	ENSP00000359184.3:n.4482-40_4482-39insAAA...
NM_000028.2:c.4482-40_4482-39insAAACTA	NP_000019.2:n.4482-40_4482-39insAAACTA
NM_000642.2:c.4482-40_4482-39insAAACTA	NP_000633.2:n.4482-40_4482-39insAAACTA
NM_000643.2:c.4482-40_4482-39insAAACTA	NP_000634.2:n.4482-40_4482-39insAAACTA
NM_000644.2:c.4482-40_4482-39insAAACTA	NP_000635.2:n.4482-40_4482-39insAAACTA
NM_000645.2:c.4431-40_4431-39insAAACTA	NP_000636.2:n.4431-40_4431-39insAAACTA
NM_000646.2:c.4434-40_4434-39insAAACTA	NP_000637.2:n.4434-40_4434-39insAAACTA
XM_005270557.1:c.4482-40_4482-39insAAACTA	XP_005270614.1:n.4482-40_4482-39insAAACTA...
XR_947626.1:n.1317+2743_1317+2744insTAGTTT
XR_947627.1:n.1206+2743_1206+2744insTAGTTT
XR_947628.1:n.1311+2743_1311+2744insTAGTTT
XR_947630.1:n.1249+2743_1249+2744insTAGTTT
XR_947632.1:n.1135+2743_1135+2744insTAGTTT
XR_947633.1:n.1246+2743_1246+2744insTAGTTT
XR_947634.1:n.660+2743_660+2744insTAGTTT
XR_947635.1:n.728+2743_728+2744insTAGTTT
XM_005270557.2:c.4482-40_4482-39insAAACTA	XP_005270614.1:n.4482-40_4482-39insAAACTA...
XM_017000501.2:c.2742-40_2742-39insAAACTA	XP_016855990.1:n.2742-40_2742-39insAAACTA...
NM_000642.3:c.4482-40_4482-39insAAACTA MANE Select	NP_000633.2:n.4482-40_4482-39insAAACTA