Canonical Allele Identifier: CA1183945504

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99915227_99915233delinsGTCAGCC , CM000663.2:g.99915227_99915233delinsGTCAGCC	GRCh38
NC_000001.10:g.100380783_100380789delinsGTCAGCC , CM000663.1:g.100380783_100380789delinsGTCAGCC	GRCh37
NC_000001.9:g.100153371_100153377delinsGTCAGCC	NCBI36
NG_012865.1:g.70144_70150delinsGTCAGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.4162-162_4162-156delinsGTCAGCC MANE Select	ENSP00000355106.3:n.4162-162_4162-156delinsGTCAGCC
ENST00000637337.1:n.4373-162_4373-156delinsGTCAGCC
ENST00000294724.8:c.4162-162_4162-156delinsGTCAGCC	ENSP00000294724.4:n.4162-162_4162-156delinsGTCAGCC
ENST00000361302.7:c.4114-162_4114-156delinsGTCAGCC	ENSP00000354971.3:n.4114-162_4114-156delinsGTCAGCC
ENST00000361522.4:c.4111-162_4111-156delinsGTCAGCC	ENSP00000354635.4:n.4111-162_4111-156delinsGTCAGCC
ENST00000361915.7:c.4162-162_4162-156delinsGTCAGCC	ENSP00000355106.3:n.4162-162_4162-156delinsGTCAGCC
ENST00000370161.6:c.4114-162_4114-156delinsGTCAGCC	ENSP00000359180.2:n.4114-162_4114-156delinsGTCAGCC
ENST00000370163.7:c.4162-162_4162-156delinsGTCAGCC	ENSP00000359182.3:n.4162-162_4162-156delinsGTCAGCC
ENST00000370165.7:c.4162-162_4162-156delinsGTCAGCC	ENSP00000359184.3:n.4162-162_4162-156delinsGTCAGCC
NM_000028.2:c.4162-162_4162-156delinsGTCAGCC	NP_000019.2:n.4162-162_4162-156delinsGTCAGCC
NM_000642.2:c.4162-162_4162-156delinsGTCAGCC	NP_000633.2:n.4162-162_4162-156delinsGTCAGCC
NM_000643.2:c.4162-162_4162-156delinsGTCAGCC	NP_000634.2:n.4162-162_4162-156delinsGTCAGCC
NM_000644.2:c.4162-162_4162-156delinsGTCAGCC	NP_000635.2:n.4162-162_4162-156delinsGTCAGCC
NM_000645.2:c.4111-162_4111-156delinsGTCAGCC	NP_000636.2:n.4111-162_4111-156delinsGTCAGCC
NM_000646.2:c.4114-162_4114-156delinsGTCAGCC	NP_000637.2:n.4114-162_4114-156delinsGTCAGCC
XM_005270557.1:c.4162-162_4162-156delinsGTCAGCC	XP_005270614.1:n.4162-162_4162-156delinsGTCAGCC
XR_947626.1:n.1318-2016_1318-2010delinsGGCTGAC
XR_947627.1:n.1207-2016_1207-2010delinsGGCTGAC
XR_947628.1:n.1312-2016_1312-2010delinsGGCTGAC
XR_947630.1:n.1250-2016_1250-2010delinsGGCTGAC
XR_947632.1:n.1136-2016_1136-2010delinsGGCTGAC
XR_947633.1:n.1247-2016_1247-2010delinsGGCTGAC
XR_947634.1:n.661-2016_661-2010delinsGGCTGAC
XR_947635.1:n.729-2016_729-2010delinsGGCTGAC
XM_005270557.2:c.4162-162_4162-156delinsGTCAGCC	XP_005270614.1:n.4162-162_4162-156delinsGTCAGCC
XM_017000501.2:c.2422-162_2422-156delinsGTCAGCC	XP_016855990.1:n.2422-162_2422-156delinsGTCAGCC
NM_000642.3:c.4162-162_4162-156delinsGTCAGCC MANE Select	NP_000633.2:n.4162-162_4162-156delinsGTCAGCC