Canonical Allele Identifier: CA2580063387

Gene: AGL

Linked Data

• ClinVar Variation Id: 1994022
• ClinVar RCV Id: RCV002806549

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99870577_99870610del , CM000663.2:g.99870577_99870610del	GRCh38
NC_000001.10:g.100336133_100336166del , CM000663.1:g.100336133_100336166del	GRCh37
NC_000001.9:g.100108721_100108754del	NCBI36
NG_012865.1:g.25494_25527del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.842_846+29del
ENST00000637337.1:n.1053_1057+29del
ENST00000294724.8:c.842_846+29del
ENST00000361302.7:c.794_798+29del
ENST00000361522.4:c.791_795+29del
ENST00000361915.7:c.842_846+29del
ENST00000370161.6:c.794_798+29del
ENST00000370163.7:c.842_846+29del
ENST00000370165.7:c.842_846+29del
NM_000028.2:c.842_846+29del
NM_000642.2:c.842_846+29del
NM_000643.2:c.842_846+29del
NM_000644.2:c.842_846+29del
NM_000645.2:c.791_795+29del
NM_000646.2:c.794_798+29del
XM_005270557.1:c.842_846+29del
XM_005270557.2:c.842_846+29del
NM_000642.3:c.842_846+29del