Canonical Allele Identifier: CA1515649805
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442415C= , CM000666.2:g.177442415C= GRCh38
NC_000004.11:g.178363569C= , CM000666.1:g.178363569C= GRCh37
NC_000004.10:g.178600563C= NCBI36
NG_011845.2:g.5089G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-40G= MANE Select ENSP00000264595.2:n.-40G=
ENST00000264595.6:c.-40G= ENSP00000264595.2:n.-40G=
NM_000027.3:c.-40G= NP_000018.2:n.-40G=
NM_001171988.1:c.-40G= NP_001165459.1:n.-40G=
NR_033655.1:n.89G=
XM_006714123.2:c.-40G= XP_006714186.1:n.-40G=
XR_001741155.2:n.55G=
NM_000027.4:c.-40G= MANE Select NP_000018.2:n.-40G=
NM_001171988.2:c.-40G= NP_001165459.1:n.-40G=
NR_033655.2:n.23G=