Canonical Allele Identifier: CA1515648686
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442106G= , CM000666.2:g.177442106G= GRCh38
NC_000004.11:g.178363260G= , CM000666.1:g.178363260G= GRCh37
NC_000004.10:g.178600254G= NCBI36
NG_011845.2:g.5398C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.127+143C= MANE Select ENSP00000264595.2:n.127+143C=
ENST00000264595.6:c.127+143C= ENSP00000264595.2:n.127+143C=
ENST00000506853.5:n.161+143C=
ENST00000510955.5:n.161+143C=
ENST00000511231.1:n.161+143C=
NM_000027.3:c.127+143C= NP_000018.2:n.127+143C=
NM_001171988.1:c.127+143C= NP_001165459.1:n.127+143C=
NR_033655.1:n.255+143C=
XM_006714123.2:c.127+143C= XP_006714186.1:n.127+143C=
XR_001741155.2:n.221+143C=
NM_000027.4:c.127+143C= MANE Select NP_000018.2:n.127+143C=
NM_001171988.2:c.127+143C= NP_001165459.1:n.127+143C=
NR_033655.2:n.189+143C=