Canonical Allele Identifier: CA419314513

Gene: AGL

Linked Data

• MyVariant Identifiers: chr1:g.100356909T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99891353T>A , CM000663.2:g.99891353T>A	GRCh38
NC_000001.10:g.100356909T>A , CM000663.1:g.100356909T>A	GRCh37
NC_000001.9:g.100129497T>A	NCBI36
NG_012865.1:g.46270T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.2946T>A MANE Select	ENSP00000355106.3:p.Ala982=
ENST00000637337.1:n.3157T>A
ENST00000294724.8:c.2946T>A	ENSP00000294724.4:p.Ala982=
ENST00000361302.7:c.2898T>A	ENSP00000354971.3:p.Ala966=
ENST00000361522.4:c.2895T>A	ENSP00000354635.4:p.Ala965=
ENST00000361915.7:c.2946T>A	ENSP00000355106.3:p.Ala982=
ENST00000370161.6:c.2898T>A	ENSP00000359180.2:p.Ala966=
ENST00000370163.7:c.2946T>A	ENSP00000359182.3:p.Ala982=
ENST00000370165.7:c.2946T>A	ENSP00000359184.3:p.Ala982=
NM_000028.2:c.2946T>A	NP_000019.2:p.Ala982=
NM_000642.2:c.2946T>A	NP_000633.2:p.Ala982=
NM_000643.2:c.2946T>A	NP_000634.2:p.Ala982=
NM_000644.2:c.2946T>A	NP_000635.2:p.Ala982=
NM_000645.2:c.2895T>A	NP_000636.2:p.Ala965=
NM_000646.2:c.2898T>A	NP_000637.2:p.Ala966=
XM_005270557.1:c.2946T>A	XP_005270614.1:p.Ala982=
XM_005270557.2:c.2946T>A	XP_005270614.1:p.Ala982=
XM_017000501.2:c.1206T>A	XP_016855990.1:p.Ala402=
NM_000642.3:c.2946T>A MANE Select	NP_000633.2:p.Ala982=