Canonical Allele Identifier: CA1183928948

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99880464_99880467delinsCTTT , CM000663.2:g.99880464_99880467delinsCTTT	GRCh38
NC_000001.10:g.100346020_100346023delinsCTTT , CM000663.1:g.100346020_100346023delinsCTTT	GRCh37
NC_000001.9:g.100118608_100118611delinsCTTT	NCBI36
NG_012865.1:g.35381_35384delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1736-168_1736-165delinsCTTT MANE Select	ENSP00000355106.3:n.1736-168_1736-165delinsCTTT
ENST00000637337.1:n.1947-168_1947-165delinsCTTT
ENST00000294724.8:c.1736-168_1736-165delinsCTTT	ENSP00000294724.4:n.1736-168_1736-165delinsCTTT
ENST00000361302.7:c.1688-168_1688-165delinsCTTT	ENSP00000354971.3:n.1688-168_1688-165delinsCTTT
ENST00000361522.4:c.1685-168_1685-165delinsCTTT	ENSP00000354635.4:n.1685-168_1685-165delinsCTTT
ENST00000361915.7:c.1736-168_1736-165delinsCTTT	ENSP00000355106.3:n.1736-168_1736-165delinsCTTT
ENST00000370161.6:c.1688-168_1688-165delinsCTTT	ENSP00000359180.2:n.1688-168_1688-165delinsCTTT
ENST00000370163.7:c.1736-168_1736-165delinsCTTT	ENSP00000359182.3:n.1736-168_1736-165delinsCTTT
ENST00000370165.7:c.1736-168_1736-165delinsCTTT	ENSP00000359184.3:n.1736-168_1736-165delinsCTTT
NM_000028.2:c.1736-168_1736-165delinsCTTT	NP_000019.2:n.1736-168_1736-165delinsCTTT
NM_000642.2:c.1736-168_1736-165delinsCTTT	NP_000633.2:n.1736-168_1736-165delinsCTTT
NM_000643.2:c.1736-168_1736-165delinsCTTT	NP_000634.2:n.1736-168_1736-165delinsCTTT
NM_000644.2:c.1736-168_1736-165delinsCTTT	NP_000635.2:n.1736-168_1736-165delinsCTTT
NM_000645.2:c.1685-168_1685-165delinsCTTT	NP_000636.2:n.1685-168_1685-165delinsCTTT
NM_000646.2:c.1688-168_1688-165delinsCTTT	NP_000637.2:n.1688-168_1688-165delinsCTTT
XM_005270557.1:c.1736-168_1736-165delinsCTTT	XP_005270614.1:n.1736-168_1736-165delinsCTTT
XM_005270557.2:c.1736-168_1736-165delinsCTTT	XP_005270614.1:n.1736-168_1736-165delinsCTTT
XM_017000501.2:c.-5-168_-5-165delinsCTTT	XP_016855990.1:n.-5-168_-5-165delinsCTTT
NM_000642.3:c.1736-168_1736-165delinsCTTT MANE Select	NP_000633.2:n.1736-168_1736-165delinsCTTT