Canonical Allele Identifier: CA1515637610
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434423T= , CM000666.2:g.177434423T= GRCh38
NC_000004.11:g.178355577T= , CM000666.1:g.178355577T= GRCh37
NC_000004.10:g.178592571T= NCBI36
NG_011845.2:g.13081A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.765A= MANE Select ENSP00000264595.2:p.Ala255=
ENST00000264595.6:c.765A= ENSP00000264595.2:p.Ala255=
ENST00000502310.5:c.336A= ENSP00000423798.1:p.Ala112=
ENST00000506853.5:n.723A=
NM_000027.3:c.765A= NP_000018.2:p.Ala255=
NM_001171988.1:c.735A= NP_001165459.1:p.Ala245=
NR_033655.1:n.817A=
XM_006714123.2:c.*59A= XP_006714186.1:n.*59A=
XR_001741155.2:n.837A=
NM_000027.4:c.765A= MANE Select NP_000018.2:p.Ala255=
NM_001171988.2:c.735A= NP_001165459.1:p.Ala245=
NR_033655.2:n.751A=