Canonical Allele Identifier: CA341337708
Gene: AGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99910776T>A , CM000663.2:g.99910776T>A GRCh38
NC_000001.10:g.100376332T>A , CM000663.1:g.100376332T>A GRCh37
NC_000001.9:g.100148920T>A NCBI36
NG_012865.1:g.65693T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.3765T>A MANE Select ENSP00000355106.3:p.Asn1255Lys
ENST00000637337.1:n.3976T>A
ENST00000294724.8:c.3765T>A ENSP00000294724.4:p.Asn1255Lys
ENST00000361302.7:c.3717T>A ENSP00000354971.3:p.Asn1239Lys
ENST00000361522.4:c.3714T>A ENSP00000354635.4:p.Asn1238Lys
ENST00000361915.7:c.3765T>A ENSP00000355106.3:p.Asn1255Lys
ENST00000370161.6:c.3717T>A ENSP00000359180.2:p.Asn1239Lys
ENST00000370163.7:c.3765T>A ENSP00000359182.3:p.Asn1255Lys
ENST00000370165.7:c.3765T>A ENSP00000359184.3:p.Asn1255Lys
NM_000028.2:c.3765T>A NP_000019.2:p.Asn1255Lys
NM_000642.2:c.3765T>A NP_000633.2:p.Asn1255Lys
NM_000643.2:c.3765T>A NP_000634.2:p.Asn1255Lys
NM_000644.2:c.3765T>A NP_000635.2:p.Asn1255Lys
NM_000645.2:c.3714T>A NP_000636.2:p.Asn1238Lys
NM_000646.2:c.3717T>A NP_000637.2:p.Asn1239Lys
XM_005270557.1:c.3765T>A XP_005270614.1:p.Asn1255Lys
XM_005270557.2:c.3765T>A XP_005270614.1:p.Asn1255Lys
XM_017000501.2:c.2025T>A XP_016855990.1:p.Asn675Lys
NM_000642.3:c.3765T>A MANE Select NP_000633.2:p.Asn1255Lys