Canonical Allele Identifier: CA2193423951

Gene: AGBL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.86893514G= , CM000677.2:g.86893514G=	GRCh38
NC_000015.9:g.87436745G= , CM000677.1:g.87436745G=	GRCh37
NC_000015.8:g.85237749G=	NCBI36
NG_033836.1:g.756504G=
NG_033836.2:g.818707G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001386094.1:c.3159-13573G= MANE Select	NP_001373023.1:n.3159-13573G=
ENST00000614907.3:c.3159-13573G= MANE Select	ENSP00000490608.2:n.3159-13573G=
NM_152336.2:c.3084-94473G=	NP_689549.2:n.3084-94473G=
NM_152336.3:c.3222-94473G=	NP_689549.3:n.3222-94473G=
NM_152336.4:c.3222-94473G=	NP_689549.3:n.3222-94473G=
ENST00000441037.6:c.3084-94473G=	ENSP00000413001.2:n.3084-94473G=
ENST00000441037.7:c.3222-94473G=	ENSP00000413001.3:n.3222-94473G=
ENST00000681381.1:n.318-148491G=
XM_011521226.1:c.3159-13573G=	XP_011519528.1:n.3159-13573G=
XM_011521226.3:c.3159-13573G=	XP_011519528.1:n.3159-13573G=
XM_011521227.1:c.3159-135311G=	XP_011519529.1:n.3159-135311G=
XM_011521227.3:c.3159-135311G=	XP_011519529.1:n.3159-135311G=
XM_017021918.2:c.3126-13573G=	XP_016877407.1:n.3126-13573G=
XM_017021919.2:c.3075-13573G=	XP_016877408.1:n.3075-13573G=