Canonical Allele Identifier: CA913046835
Gene: AGL HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.100361931dup (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99896375dup , CM000663.2:g.99896375dup GRCh38
NC_000001.10:g.100361931dup , CM000663.1:g.100361931dup GRCh37
NC_000001.9:g.100134519dup NCBI36
NG_012865.1:g.51292dup

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.3349dup MANE Select ENSP00000355106.3:p.Tyr1117LeufsTer22
ENST00000637337.1:n.3560dup
ENST00000294724.8:c.3349dup ENSP00000294724.4:p.Tyr1117LeufsTer22
ENST00000361302.7:c.3301dup ENSP00000354971.3:p.Tyr1101LeufsTer22
ENST00000361522.4:c.3298dup ENSP00000354635.4:p.Tyr1100LeufsTer22
ENST00000361915.7:c.3349dup ENSP00000355106.3:p.Tyr1117LeufsTer22
ENST00000370161.6:c.3301dup ENSP00000359180.2:p.Tyr1101LeufsTer22
ENST00000370163.7:c.3349dup ENSP00000359182.3:p.Tyr1117LeufsTer22
ENST00000370165.7:c.3349dup ENSP00000359184.3:p.Tyr1117LeufsTer22
NM_000028.2:c.3349dup NP_000019.2:p.Tyr1117LeufsTer22
NM_000642.2:c.3349dup NP_000633.2:p.Tyr1117LeufsTer22
NM_000643.2:c.3349dup NP_000634.2:p.Tyr1117LeufsTer22
NM_000644.2:c.3349dup NP_000635.2:p.Tyr1117LeufsTer22
NM_000645.2:c.3298dup NP_000636.2:p.Tyr1100LeufsTer22
NM_000646.2:c.3301dup NP_000637.2:p.Tyr1101LeufsTer22
XM_005270557.1:c.3349dup XP_005270614.1:p.Tyr1117LeufsTer22
XM_005270557.2:c.3349dup XP_005270614.1:p.Tyr1117LeufsTer22
XM_017000501.2:c.1609dup XP_016855990.1:p.Tyr537LeufsTer22
NM_000642.3:c.3349dup MANE Select NP_000633.2:p.Tyr1117LeufsTer22