Canonical Allele Identifier: CA341345127
Gene: AGL HGNC NCBI

Linked Data

gnomAD v4: 1-99875365-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99875365A>T , CM000663.2:g.99875365A>T GRCh38
NC_000001.10:g.100340921A>T , CM000663.1:g.100340921A>T GRCh37
NC_000001.9:g.100113509A>T NCBI36
NG_012865.1:g.30282A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.1193A>T MANE Select ENSP00000355106.3:p.Asn398Ile
ENST00000637337.1:n.1404A>T
ENST00000294724.8:c.1193A>T ENSP00000294724.4:p.Asn398Ile
ENST00000361302.7:c.1145A>T ENSP00000354971.3:p.Asn382Ile
ENST00000361522.4:c.1142A>T ENSP00000354635.4:p.Asn381Ile
ENST00000361915.7:c.1193A>T ENSP00000355106.3:p.Asn398Ile
ENST00000370161.6:c.1145A>T ENSP00000359180.2:p.Asn382Ile
ENST00000370163.7:c.1193A>T ENSP00000359182.3:p.Asn398Ile
ENST00000370165.7:c.1193A>T ENSP00000359184.3:p.Asn398Ile
ENST00000477753.1:n.452A>T
NM_000028.2:c.1193A>T NP_000019.2:p.Asn398Ile
NM_000642.2:c.1193A>T NP_000633.2:p.Asn398Ile
NM_000643.2:c.1193A>T NP_000634.2:p.Asn398Ile
NM_000644.2:c.1193A>T NP_000635.2:p.Asn398Ile
NM_000645.2:c.1142A>T NP_000636.2:p.Asn381Ile
NM_000646.2:c.1145A>T NP_000637.2:p.Asn382Ile
XM_005270557.1:c.1193A>T XP_005270614.1:p.Asn398Ile
XM_005270557.2:c.1193A>T XP_005270614.1:p.Asn398Ile
NM_000642.3:c.1193A>T MANE Select NP_000633.2:p.Asn398Ile