Canonical Allele Identifier: CA1515649808
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442416A= , CM000666.2:g.177442416A= GRCh38
NC_000004.11:g.178363570A= , CM000666.1:g.178363570A= GRCh37
NC_000004.10:g.178600564A= NCBI36
NG_011845.2:g.5088T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-41T= MANE Select ENSP00000264595.2:n.-41T=
ENST00000264595.6:c.-41T= ENSP00000264595.2:n.-41T=
NM_000027.3:c.-41T= NP_000018.2:n.-41T=
NM_001171988.1:c.-41T= NP_001165459.1:n.-41T=
NR_033655.1:n.88T=
XM_006714123.2:c.-41T= XP_006714186.1:n.-41T=
XR_001741155.2:n.54T=
NM_000027.4:c.-41T= MANE Select NP_000018.2:n.-41T=
NM_001171988.2:c.-41T= NP_001165459.1:n.-41T=
NR_033655.2:n.22T=