Canonical Allele Identifier: CA2764653782
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439725T>G , CM000666.2:g.177439725T>G GRCh38
NC_000004.11:g.178360879T>G , CM000666.1:g.178360879T>G GRCh37
NC_000004.10:g.178597873T>G NCBI36
NG_011845.2:g.7779A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.282-37A>C MANE Select ENSP00000264595.2:n.282-37A>C
ENST00000264595.6:c.282-37A>C ENSP00000264595.2:n.282-37A>C
ENST00000506853.5:n.316-37A>C
ENST00000510955.5:n.315+548A>C
NM_000027.3:c.282-37A>C NP_000018.2:n.282-37A>C
NM_001171988.1:c.282-37A>C NP_001165459.1:n.282-37A>C
NR_033655.1:n.410-37A>C
XM_006714123.2:c.282-37A>C XP_006714186.1:n.282-37A>C
XR_001741155.2:n.376-37A>C
NM_000027.4:c.282-37A>C MANE Select NP_000018.2:n.282-37A>C
NM_001171988.2:c.282-37A>C NP_001165459.1:n.282-37A>C
NR_033655.2:n.344-37A>C