Canonical Allele Identifier: CA341323454

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99851058C>G , CM000663.2:g.99851058C>G	GRCh38
NC_000001.10:g.100316614C>G , CM000663.1:g.100316614C>G	GRCh37
NC_000001.9:g.100089202C>G	NCBI36
NG_012865.1:g.5975C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.16C>G MANE Select	ENSP00000355106.3:p.Gln6Glu
ENST00000294724.8:c.16C>G	ENSP00000294724.4:p.Gln6Glu
ENST00000361302.7:c.-176C>G	ENSP00000354971.3:n.-176C>G
ENST00000361915.7:c.16C>G	ENSP00000355106.3:p.Gln6Glu
ENST00000370163.7:c.16C>G	ENSP00000359182.3:p.Gln6Glu
ENST00000370165.7:c.16C>G	ENSP00000359184.3:p.Gln6Glu
NM_000028.2:c.16C>G	NP_000019.2:p.Gln6Glu
NM_000642.2:c.16C>G	NP_000633.2:p.Gln6Glu
NM_000643.2:c.16C>G	NP_000634.2:p.Gln6Glu
NM_000644.2:c.16C>G	NP_000635.2:p.Gln6Glu
NM_000646.2:c.-176C>G	NP_000637.2:n.-176C>G
XM_005270557.1:c.16C>G	XP_005270614.1:p.Gln6Glu
XM_005270557.2:c.16C>G	XP_005270614.1:p.Gln6Glu
NM_000642.3:c.16C>G MANE Select	NP_000633.2:p.Gln6Glu