Canonical Allele Identifier: CA419096019

Gene: AGL

Linked Data

• MyVariant Identifiers: chr1:g.100329964C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99864408C>G , CM000663.2:g.99864408C>G	GRCh38
NC_000001.10:g.100329964C>G , CM000663.1:g.100329964C>G	GRCh37
NC_000001.9:g.100102552C>G	NCBI36
NG_012865.1:g.19325C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.483C>G MANE Select	ENSP00000355106.3:p.Thr161=
ENST00000637337.1:n.694C>G
ENST00000294724.8:c.483C>G	ENSP00000294724.4:p.Thr161=
ENST00000361302.7:c.435C>G	ENSP00000354971.3:p.Thr145=
ENST00000361522.4:c.432C>G	ENSP00000354635.4:p.Thr144=
ENST00000361915.7:c.483C>G	ENSP00000355106.3:p.Thr161=
ENST00000370161.6:c.435C>G	ENSP00000359180.2:p.Thr145=
ENST00000370163.7:c.483C>G	ENSP00000359182.3:p.Thr161=
ENST00000370165.7:c.483C>G	ENSP00000359184.3:p.Thr161=
NM_000028.2:c.483C>G	NP_000019.2:p.Thr161=
NM_000642.2:c.483C>G	NP_000633.2:p.Thr161=
NM_000643.2:c.483C>G	NP_000634.2:p.Thr161=
NM_000644.2:c.483C>G	NP_000635.2:p.Thr161=
NM_000645.2:c.432C>G	NP_000636.2:p.Thr144=
NM_000646.2:c.435C>G	NP_000637.2:p.Thr145=
XM_005270557.1:c.483C>G	XP_005270614.1:p.Thr161=
XM_005270557.2:c.483C>G	XP_005270614.1:p.Thr161=
NM_000642.3:c.483C>G MANE Select	NP_000633.2:p.Thr161=