Canonical Allele Identifier: CA1515649546
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442352A= , CM000666.2:g.177442352A= GRCh38
NC_000004.11:g.178363506A= , CM000666.1:g.178363506A= GRCh37
NC_000004.10:g.178600500A= NCBI36
NG_011845.2:g.5152T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.24T= MANE Select ENSP00000264595.2:p.Pro8=
ENST00000264595.6:c.24T= ENSP00000264595.2:p.Pro8=
ENST00000506853.5:n.58T=
ENST00000510955.5:n.58T=
ENST00000511231.1:n.58T=
NM_000027.3:c.24T= NP_000018.2:p.Pro8=
NM_001171988.1:c.24T= NP_001165459.1:p.Pro8=
NR_033655.1:n.152T=
XM_006714123.2:c.24T= XP_006714186.1:p.Pro8=
XR_001741155.2:n.118T=
NM_000027.4:c.24T= MANE Select NP_000018.2:p.Pro8=
NM_001171988.2:c.24T= NP_001165459.1:p.Pro8=
NR_033655.2:n.86T=