Canonical Allele Identifier: CA1515649775
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442405A= , CM000666.2:g.177442405A= GRCh38
NC_000004.11:g.178363559A= , CM000666.1:g.178363559A= GRCh37
NC_000004.10:g.178600553A= NCBI36
NG_011845.2:g.5099T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-30T= MANE Select ENSP00000264595.2:n.-30T=
ENST00000264595.6:c.-30T= ENSP00000264595.2:n.-30T=
ENST00000506853.5:n.5T=
ENST00000510955.5:n.5T=
ENST00000511231.1:n.5T=
NM_000027.3:c.-30T= NP_000018.2:n.-30T=
NM_001171988.1:c.-30T= NP_001165459.1:n.-30T=
NR_033655.1:n.99T=
XM_006714123.2:c.-30T= XP_006714186.1:n.-30T=
XR_001741155.2:n.65T=
NM_000027.4:c.-30T= MANE Select NP_000018.2:n.-30T=
NM_001171988.2:c.-30T= NP_001165459.1:n.-30T=
NR_033655.2:n.33T=