Canonical Allele Identifier: CA1515643523
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177438802A= , CM000666.2:g.177438802A= GRCh38
NC_000004.11:g.178359956A= , CM000666.1:g.178359956A= GRCh37
NC_000004.10:g.178596950A= NCBI36
NG_011845.2:g.8702T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.450T= MANE Select ENSP00000264595.2:p.Ala150=
ENST00000264595.6:c.450T= ENSP00000264595.2:p.Ala150=
ENST00000502310.5:c.105T= ENSP00000423798.1:p.Ala35=
ENST00000506853.5:n.484T=
ENST00000510635.1:c.146T=
ENST00000510955.5:n.371T=
NM_000027.3:c.450T= NP_000018.2:p.Ala150=
NM_001171988.1:c.450T= NP_001165459.1:p.Ala150=
NR_033655.1:n.578T=
XM_006714123.2:c.450T= XP_006714186.1:p.Ala150=
XR_001741155.2:n.544T=
NM_000027.4:c.450T= MANE Select NP_000018.2:p.Ala150=
NM_001171988.2:c.450T= NP_001165459.1:p.Ala150=
NR_033655.2:n.512T=