Canonical Allele Identifier: CA419084470

Gene: AGL

Linked Data

• MyVariant Identifiers: chr1:g.100357287G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99891731G>A , CM000663.2:g.99891731G>A	GRCh38
NC_000001.10:g.100357287G>A , CM000663.1:g.100357287G>A	GRCh37
NC_000001.9:g.100129875G>A	NCBI36
NG_012865.1:g.46648G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.3075G>A MANE Select	ENSP00000355106.3:p.Gln1025=
ENST00000637337.1:n.3286G>A
ENST00000294724.8:c.3075G>A	ENSP00000294724.4:p.Gln1025=
ENST00000361302.7:c.3027G>A	ENSP00000354971.3:p.Gln1009=
ENST00000361522.4:c.3024G>A	ENSP00000354635.4:p.Gln1008=
ENST00000361915.7:c.3075G>A	ENSP00000355106.3:p.Gln1025=
ENST00000370161.6:c.3027G>A	ENSP00000359180.2:p.Gln1009=
ENST00000370163.7:c.3075G>A	ENSP00000359182.3:p.Gln1025=
ENST00000370165.7:c.3075G>A	ENSP00000359184.3:p.Gln1025=
NM_000028.2:c.3075G>A	NP_000019.2:p.Gln1025=
NM_000642.2:c.3075G>A	NP_000633.2:p.Gln1025=
NM_000643.2:c.3075G>A	NP_000634.2:p.Gln1025=
NM_000644.2:c.3075G>A	NP_000635.2:p.Gln1025=
NM_000645.2:c.3024G>A	NP_000636.2:p.Gln1008=
NM_000646.2:c.3027G>A	NP_000637.2:p.Gln1009=
XM_005270557.1:c.3075G>A	XP_005270614.1:p.Gln1025=
XM_005270557.2:c.3075G>A	XP_005270614.1:p.Gln1025=
XM_017000501.2:c.1335G>A	XP_016855990.1:p.Gln445=
NM_000642.3:c.3075G>A MANE Select	NP_000633.2:p.Gln1025=