Canonical Allele Identifier: CA341343732
Gene: AGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99921597T>A , CM000663.2:g.99921597T>A GRCh38
NC_000001.10:g.100387153T>A , CM000663.1:g.100387153T>A GRCh37
NC_000001.9:g.100159741T>A NCBI36
NG_012865.1:g.76514T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.4545T>A MANE Select ENSP00000355106.3:p.Cys1515Ter
ENST00000637337.1:n.4756T>A
ENST00000294724.8:c.4545T>A ENSP00000294724.4:p.Cys1515Ter
ENST00000361302.7:c.4497T>A ENSP00000354971.3:p.Cys1499Ter
ENST00000361522.4:c.4494T>A ENSP00000354635.4:p.Cys1498Ter
ENST00000361915.7:c.4545T>A ENSP00000355106.3:p.Cys1515Ter
ENST00000370161.6:c.4497T>A ENSP00000359180.2:p.Cys1499Ter
ENST00000370163.7:c.4545T>A ENSP00000359182.3:p.Cys1515Ter
ENST00000370165.7:c.4545T>A ENSP00000359184.3:p.Cys1515Ter
NM_000028.2:c.4545T>A NP_000019.2:p.Cys1515Ter
NM_000642.2:c.4545T>A NP_000633.2:p.Cys1515Ter
NM_000643.2:c.4545T>A NP_000634.2:p.Cys1515Ter
NM_000644.2:c.4545T>A NP_000635.2:p.Cys1515Ter
NM_000645.2:c.4494T>A NP_000636.2:p.Cys1498Ter
NM_000646.2:c.4497T>A NP_000637.2:p.Cys1499Ter
XM_005270557.1:c.4545T>A XP_005270614.1:p.Cys1515Ter
XR_947626.1:n.1317+2641A>T
XR_947627.1:n.1206+2641A>T
XR_947628.1:n.1311+2641A>T
XR_947630.1:n.1249+2641A>T
XR_947632.1:n.1135+2641A>T
XR_947633.1:n.1246+2641A>T
XR_947634.1:n.660+2641A>T
XR_947635.1:n.728+2641A>T
XM_005270557.2:c.4545T>A XP_005270614.1:p.Cys1515Ter
XM_017000501.2:c.2805T>A XP_016855990.1:p.Cys935Ter
NM_000642.3:c.4545T>A MANE Select NP_000633.2:p.Cys1515Ter