Canonical Allele Identifier: CA1183928983

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99880540_99880543delinsCTTT , CM000663.2:g.99880540_99880543delinsCTTT	GRCh38
NC_000001.10:g.100346096_100346099delinsCTTT , CM000663.1:g.100346096_100346099delinsCTTT	GRCh37
NC_000001.9:g.100118684_100118687delinsCTTT	NCBI36
NG_012865.1:g.35457_35460delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1736-92_1736-89delinsCTTT MANE Select	ENSP00000355106.3:n.1736-92_1736-89delinsCTTT
ENST00000637337.1:n.1947-92_1947-89delinsCTTT
ENST00000294724.8:c.1736-92_1736-89delinsCTTT	ENSP00000294724.4:n.1736-92_1736-89delinsCTTT
ENST00000361302.7:c.1688-92_1688-89delinsCTTT	ENSP00000354971.3:n.1688-92_1688-89delinsCTTT
ENST00000361522.4:c.1685-92_1685-89delinsCTTT	ENSP00000354635.4:n.1685-92_1685-89delinsCTTT
ENST00000361915.7:c.1736-92_1736-89delinsCTTT	ENSP00000355106.3:n.1736-92_1736-89delinsCTTT
ENST00000370161.6:c.1688-92_1688-89delinsCTTT	ENSP00000359180.2:n.1688-92_1688-89delinsCTTT
ENST00000370163.7:c.1736-92_1736-89delinsCTTT	ENSP00000359182.3:n.1736-92_1736-89delinsCTTT
ENST00000370165.7:c.1736-92_1736-89delinsCTTT	ENSP00000359184.3:n.1736-92_1736-89delinsCTTT
NM_000028.2:c.1736-92_1736-89delinsCTTT	NP_000019.2:n.1736-92_1736-89delinsCTTT
NM_000642.2:c.1736-92_1736-89delinsCTTT	NP_000633.2:n.1736-92_1736-89delinsCTTT
NM_000643.2:c.1736-92_1736-89delinsCTTT	NP_000634.2:n.1736-92_1736-89delinsCTTT
NM_000644.2:c.1736-92_1736-89delinsCTTT	NP_000635.2:n.1736-92_1736-89delinsCTTT
NM_000645.2:c.1685-92_1685-89delinsCTTT	NP_000636.2:n.1685-92_1685-89delinsCTTT
NM_000646.2:c.1688-92_1688-89delinsCTTT	NP_000637.2:n.1688-92_1688-89delinsCTTT
XM_005270557.1:c.1736-92_1736-89delinsCTTT	XP_005270614.1:n.1736-92_1736-89delinsCTTT
XM_005270557.2:c.1736-92_1736-89delinsCTTT	XP_005270614.1:n.1736-92_1736-89delinsCTTT
XM_017000501.2:c.-5-92_-5-89delinsCTTT	XP_016855990.1:n.-5-92_-5-89delinsCTTT
NM_000642.3:c.1736-92_1736-89delinsCTTT MANE Select	NP_000633.2:n.1736-92_1736-89delinsCTTT