Canonical Allele Identifier: CA2570546688

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921527_99921528del , CM000663.2:g.99921527_99921528del	GRCh38
NC_000001.10:g.100387083_100387084del , CM000663.1:g.100387083_100387084del	GRCh37
NC_000001.9:g.100159671_100159672del	NCBI36
NG_012865.1:g.76444_76445del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.4482-7_4482-6del MANE Select	ENSP00000355106.3:n.4482-7_4482-6del
ENST00000637337.1:n.4693-7_4693-6del
ENST00000294724.8:c.4482-7_4482-6del	ENSP00000294724.4:n.4482-7_4482-6del
ENST00000361302.7:c.4434-7_4434-6del	ENSP00000354971.3:n.4434-7_4434-6del
ENST00000361522.4:c.4431-7_4431-6del	ENSP00000354635.4:n.4431-7_4431-6del
ENST00000361915.7:c.4482-7_4482-6del	ENSP00000355106.3:n.4482-7_4482-6del
ENST00000370161.6:c.4434-7_4434-6del	ENSP00000359180.2:n.4434-7_4434-6del
ENST00000370163.7:c.4482-7_4482-6del	ENSP00000359182.3:n.4482-7_4482-6del
ENST00000370165.7:c.4482-7_4482-6del	ENSP00000359184.3:n.4482-7_4482-6del
NM_000028.2:c.4482-7_4482-6del	NP_000019.2:n.4482-7_4482-6del
NM_000642.2:c.4482-7_4482-6del	NP_000633.2:n.4482-7_4482-6del
NM_000643.2:c.4482-7_4482-6del	NP_000634.2:n.4482-7_4482-6del
NM_000644.2:c.4482-7_4482-6del	NP_000635.2:n.4482-7_4482-6del
NM_000645.2:c.4431-7_4431-6del	NP_000636.2:n.4431-7_4431-6del
NM_000646.2:c.4434-7_4434-6del	NP_000637.2:n.4434-7_4434-6del
XM_005270557.1:c.4482-7_4482-6del	XP_005270614.1:n.4482-7_4482-6del
XR_947626.1:n.1317+2710_1317+2711del
XR_947627.1:n.1206+2710_1206+2711del
XR_947628.1:n.1311+2710_1311+2711del
XR_947630.1:n.1249+2710_1249+2711del
XR_947632.1:n.1135+2710_1135+2711del
XR_947633.1:n.1246+2710_1246+2711del
XR_947634.1:n.660+2710_660+2711del
XR_947635.1:n.728+2710_728+2711del
XM_005270557.2:c.4482-7_4482-6del	XP_005270614.1:n.4482-7_4482-6del
XM_017000501.2:c.2742-7_2742-6del	XP_016855990.1:n.2742-7_2742-6del
NM_000642.3:c.4482-7_4482-6del MANE Select	NP_000633.2:n.4482-7_4482-6del