Canonical Allele Identifier: CA1183929329

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99881445C= , CM000663.2:g.99881445C=	GRCh38
NC_000001.10:g.100347001C= , CM000663.1:g.100347001C=	GRCh37
NC_000001.9:g.100119589C=	NCBI36
NG_012865.1:g.36362C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.2155C= MANE Select	ENSP00000355106.3:p.Gln719=
ENST00000637337.1:n.2366C=
ENST00000294724.8:c.2155C=	ENSP00000294724.4:p.Gln719=
ENST00000361302.7:c.2107C=	ENSP00000354971.3:p.Gln703=
ENST00000361522.4:c.2104C=	ENSP00000354635.4:p.Gln702=
ENST00000361915.7:c.2155C=	ENSP00000355106.3:p.Gln719=
ENST00000370161.6:c.2107C=	ENSP00000359180.2:p.Gln703=
ENST00000370163.7:c.2155C=	ENSP00000359182.3:p.Gln719=
ENST00000370165.7:c.2155C=	ENSP00000359184.3:p.Gln719=
NM_000028.2:c.2155C=	NP_000019.2:p.Gln719=
NM_000642.2:c.2155C=	NP_000633.2:p.Gln719=
NM_000643.2:c.2155C=	NP_000634.2:p.Gln719=
NM_000644.2:c.2155C=	NP_000635.2:p.Gln719=
NM_000645.2:c.2104C=	NP_000636.2:p.Gln702=
NM_000646.2:c.2107C=	NP_000637.2:p.Gln703=
XM_005270557.1:c.2155C=	XP_005270614.1:p.Gln719=
XM_005270557.2:c.2155C=	XP_005270614.1:p.Gln719=
XM_017000501.2:c.415C=	XP_016855990.1:p.Gln139=
NM_000642.3:c.2155C= MANE Select	NP_000633.2:p.Gln719=