Canonical Allele Identifier: CA1183945542

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99915272_99915273delinsTC , CM000663.2:g.99915272_99915273delinsTC	GRCh38
NC_000001.10:g.100380828_100380829delinsTC , CM000663.1:g.100380828_100380829delinsTC	GRCh37
NC_000001.9:g.100153416_100153417delinsTC	NCBI36
NG_012865.1:g.70189_70190delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.4162-117_4162-116delinsTC MANE Select	ENSP00000355106.3:n.4162-117_4162-116deli...
ENST00000637337.1:n.4373-117_4373-116delinsTC
ENST00000294724.8:c.4162-117_4162-116delinsTC	ENSP00000294724.4:n.4162-117_4162-116deli...
ENST00000361302.7:c.4114-117_4114-116delinsTC	ENSP00000354971.3:n.4114-117_4114-116deli...
ENST00000361522.4:c.4111-117_4111-116delinsTC	ENSP00000354635.4:n.4111-117_4111-116deli...
ENST00000361915.7:c.4162-117_4162-116delinsTC	ENSP00000355106.3:n.4162-117_4162-116deli...
ENST00000370161.6:c.4114-117_4114-116delinsTC	ENSP00000359180.2:n.4114-117_4114-116deli...
ENST00000370163.7:c.4162-117_4162-116delinsTC	ENSP00000359182.3:n.4162-117_4162-116deli...
ENST00000370165.7:c.4162-117_4162-116delinsTC	ENSP00000359184.3:n.4162-117_4162-116deli...
NM_000028.2:c.4162-117_4162-116delinsTC	NP_000019.2:n.4162-117_4162-116delinsTC
NM_000642.2:c.4162-117_4162-116delinsTC	NP_000633.2:n.4162-117_4162-116delinsTC
NM_000643.2:c.4162-117_4162-116delinsTC	NP_000634.2:n.4162-117_4162-116delinsTC
NM_000644.2:c.4162-117_4162-116delinsTC	NP_000635.2:n.4162-117_4162-116delinsTC
NM_000645.2:c.4111-117_4111-116delinsTC	NP_000636.2:n.4111-117_4111-116delinsTC
NM_000646.2:c.4114-117_4114-116delinsTC	NP_000637.2:n.4114-117_4114-116delinsTC
XM_005270557.1:c.4162-117_4162-116delinsTC	XP_005270614.1:n.4162-117_4162-116delinsT...
XR_947626.1:n.1318-2056_1318-2055delinsGA
XR_947627.1:n.1207-2056_1207-2055delinsGA
XR_947628.1:n.1312-2056_1312-2055delinsGA
XR_947630.1:n.1250-2056_1250-2055delinsGA
XR_947632.1:n.1136-2056_1136-2055delinsGA
XR_947633.1:n.1247-2056_1247-2055delinsGA
XR_947634.1:n.661-2056_661-2055delinsGA
XR_947635.1:n.729-2056_729-2055delinsGA
XM_005270557.2:c.4162-117_4162-116delinsTC	XP_005270614.1:n.4162-117_4162-116delinsT...
XM_017000501.2:c.2422-117_2422-116delinsTC	XP_016855990.1:n.2422-117_2422-116delinsT...
NM_000642.3:c.4162-117_4162-116delinsTC MANE Select	NP_000633.2:n.4162-117_4162-116delinsTC