Canonical Allele Identifier: CA341331306
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 2190285
ClinVar RCV Id: RCV002627985
dbSNP Id: rs1188420969
gnomAD v3: 1-99900719-A-G
gnomAD v4: 1-99900719-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99900719A>G , CM000663.2:g.99900719A>G GRCh38
NC_000001.10:g.100366275A>G , CM000663.1:g.100366275A>G GRCh37
NC_000001.9:g.100138863A>G NCBI36
NG_012865.1:g.55636A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.3446A>G MANE Select ENSP00000355106.3:p.Asn1149Ser
ENST00000637337.1:n.3657A>G
ENST00000294724.8:c.3446A>G ENSP00000294724.4:p.Asn1149Ser
ENST00000361302.7:c.3398A>G ENSP00000354971.3:p.Asn1133Ser
ENST00000361522.4:c.3395A>G ENSP00000354635.4:p.Asn1132Ser
ENST00000361915.7:c.3446A>G ENSP00000355106.3:p.Asn1149Ser
ENST00000370161.6:c.3398A>G ENSP00000359180.2:p.Asn1133Ser
ENST00000370163.7:c.3446A>G ENSP00000359182.3:p.Asn1149Ser
ENST00000370165.7:c.3446A>G ENSP00000359184.3:p.Asn1149Ser
NM_000028.2:c.3446A>G NP_000019.2:p.Asn1149Ser
NM_000642.2:c.3446A>G NP_000633.2:p.Asn1149Ser
NM_000643.2:c.3446A>G NP_000634.2:p.Asn1149Ser
NM_000644.2:c.3446A>G NP_000635.2:p.Asn1149Ser
NM_000645.2:c.3395A>G NP_000636.2:p.Asn1132Ser
NM_000646.2:c.3398A>G NP_000637.2:p.Asn1133Ser
XM_005270557.1:c.3446A>G XP_005270614.1:p.Asn1149Ser
XM_005270557.2:c.3446A>G XP_005270614.1:p.Asn1149Ser
XM_017000501.2:c.1706A>G XP_016855990.1:p.Asn569Ser
NM_000642.3:c.3446A>G MANE Select NP_000633.2:p.Asn1149Ser