Canonical Allele Identifier: CA1515641837
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437438C= , CM000666.2:g.177437438C= GRCh38
NC_000004.11:g.178358592C= , CM000666.1:g.178358592C= GRCh37
NC_000004.10:g.178595586C= NCBI36
NG_011845.2:g.10066G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.589G= MANE Select ENSP00000264595.2:p.Glu197=
ENST00000264595.6:c.589G= ENSP00000264595.2:p.Glu197=
ENST00000502310.5:c.244G= ENSP00000423798.1:p.Glu82=
ENST00000506853.5:n.623G=
ENST00000510635.1:c.285G=
ENST00000510955.5:n.510G=
NM_000027.3:c.589G= NP_000018.2:p.Glu197=
NM_001171988.1:c.589G= NP_001165459.1:p.Glu197=
NR_033655.1:n.717G=
XM_006714123.2:c.589G= XP_006714186.1:p.Glu197=
XR_001741155.2:n.683G=
NM_000027.4:c.589G= MANE Select NP_000018.2:p.Glu197=
NM_001171988.2:c.589G= NP_001165459.1:p.Glu197=
NR_033655.2:n.651G=