Canonical Allele Identifier: CA7716372

Gene: AGBL1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.86674382A>G , CM000677.2:g.86674382A>G	GRCh38
NC_000015.9:g.87217613A>G , CM000677.1:g.87217613A>G	GRCh37
NC_000015.8:g.85018617A>G	NCBI36
NG_033836.1:g.537372A>G
NG_033836.2:g.599575A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441037.7:c.3167A>G	ENSP00000413001.3:p.Gln1056Arg
ENST00000614907.3:c.3104A>G MANE Select	ENSP00000490608.2:p.Gln1035Arg
ENST00000681381.1:n.263A>G
ENST00000421325.3:c.3029A>G	ENSP00000397173.3:p.Gln1010Arg
ENST00000441037.6:c.3029A>G	ENSP00000413001.2:p.Gln1010Arg
NM_152336.2:c.3029A>G	NP_689549.2:p.Gln1010Arg
XM_011521226.1:c.3104A>G	XP_011519528.1:p.Gln1035Arg
XM_011521227.1:c.3104A>G	XP_011519529.1:p.Gln1035Arg
NM_152336.3:c.3167A>G	NP_689549.3:p.Gln1056Arg
XM_011521226.3:c.3104A>G	XP_011519528.1:p.Gln1035Arg
XM_011521227.3:c.3104A>G	XP_011519529.1:p.Gln1035Arg
XM_017021918.2:c.3071A>G	XP_016877407.1:p.Gln1024Arg
XM_017021919.2:c.3020A>G	XP_016877408.1:p.Gln1007Arg
NM_152336.4:c.3167A>G	NP_689549.3:p.Gln1056Arg
NM_001386094.1:c.3104A>G MANE Select	NP_001373023.1:p.Gln1035Arg