Canonical Allele Identifier: CA1515649748
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442395C= , CM000666.2:g.177442395C= GRCh38
NC_000004.11:g.178363549C= , CM000666.1:g.178363549C= GRCh37
NC_000004.10:g.178600543C= NCBI36
NG_011845.2:g.5109G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-20G= MANE Select ENSP00000264595.2:n.-20G=
ENST00000264595.6:c.-20G= ENSP00000264595.2:n.-20G=
ENST00000506853.5:n.15G=
ENST00000510955.5:n.15G=
ENST00000511231.1:n.15G=
NM_000027.3:c.-20G= NP_000018.2:n.-20G=
NM_001171988.1:c.-20G= NP_001165459.1:n.-20G=
NR_033655.1:n.109G=
XM_006714123.2:c.-20G= XP_006714186.1:n.-20G=
XR_001741155.2:n.75G=
NM_000027.4:c.-20G= MANE Select NP_000018.2:n.-20G=
NM_001171988.2:c.-20G= NP_001165459.1:n.-20G=
NR_033655.2:n.43G=