Canonical Allele Identifier: CA1183917058

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99850929A= , CM000663.2:g.99850929A=	GRCh38
NC_000001.10:g.100316485A= , CM000663.1:g.100316485A=	GRCh37
NC_000001.9:g.100089073A=	NCBI36
NG_012865.1:g.5846A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.-68-46A= MANE Select	ENSP00000355106.3:n.-68-46A=
ENST00000294724.8:c.-69+31A=	ENSP00000294724.4:n.-69+31A=
ENST00000361915.7:c.-68-46A=	ENSP00000355106.3:n.-68-46A=
ENST00000370163.7:c.-68-46A=	ENSP00000359182.3:n.-68-46A=
ENST00000370165.7:c.-8-106A=	ENSP00000359184.3:n.-8-106A=
NM_000028.2:c.-69+31A=	NP_000019.2:n.-69+31A=
NM_000642.2:c.-68-46A=	NP_000633.2:n.-68-46A=
NM_000643.2:c.-68-46A=	NP_000634.2:n.-68-46A=
NM_000644.2:c.-8-106A=	NP_000635.2:n.-8-106A=
XM_005270557.1:c.-68-46A=	XP_005270614.1:n.-68-46A=
XM_005270557.2:c.-68-46A=	XP_005270614.1:n.-68-46A=
NM_000642.3:c.-68-46A= MANE Select	NP_000633.2:n.-68-46A=