Canonical Allele Identifier: CA1183929223

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99881174_99881175delinsTC , CM000663.2:g.99881174_99881175delinsTC	GRCh38
NC_000001.10:g.100346730_100346731delinsTC , CM000663.1:g.100346730_100346731delinsTC	GRCh37
NC_000001.9:g.100119318_100119319delinsTC	NCBI36
NG_012865.1:g.36091_36092delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.1998_1999delinsTC MANE Select	ENSP00000355106.3:p.His666=
ENST00000637337.1:n.2209_2210delinsTC
ENST00000294724.8:c.1998_1999delinsTC	ENSP00000294724.4:p.His666=
ENST00000361302.7:c.1950_1951delinsTC	ENSP00000354971.3:p.His650=
ENST00000361522.4:c.1947_1948delinsTC	ENSP00000354635.4:p.His649=
ENST00000361915.7:c.1998_1999delinsTC	ENSP00000355106.3:p.His666=
ENST00000370161.6:c.1950_1951delinsTC	ENSP00000359180.2:p.His650=
ENST00000370163.7:c.1998_1999delinsTC	ENSP00000359182.3:p.His666=
ENST00000370165.7:c.1998_1999delinsTC	ENSP00000359184.3:p.His666=
NM_000028.2:c.1998_1999delinsTC	NP_000019.2:p.His666=
NM_000642.2:c.1998_1999delinsTC	NP_000633.2:p.His666=
NM_000643.2:c.1998_1999delinsTC	NP_000634.2:p.His666=
NM_000644.2:c.1998_1999delinsTC	NP_000635.2:p.His666=
NM_000645.2:c.1947_1948delinsTC	NP_000636.2:p.His649=
NM_000646.2:c.1950_1951delinsTC	NP_000637.2:p.His650=
XM_005270557.1:c.1998_1999delinsTC	XP_005270614.1:p.His666=
XM_005270557.2:c.1998_1999delinsTC	XP_005270614.1:p.His666=
XM_017000501.2:c.258_259delinsTC	XP_016855990.1:p.His86=
NM_000642.3:c.1998_1999delinsTC MANE Select	NP_000633.2:p.His666=