Canonical Allele Identifier: CA2578238494
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177438649C>T , CM000666.2:g.177438649C>T GRCh38
NC_000004.11:g.178359803C>T , CM000666.1:g.178359803C>T GRCh37
NC_000004.10:g.178596797C>T NCBI36
NG_011845.2:g.8855G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.507+96G>A MANE Select ENSP00000264595.2:n.507+96G>A
ENST00000264595.6:c.507+96G>A ENSP00000264595.2:n.507+96G>A
ENST00000502310.5:c.162+96G>A ENSP00000423798.1:n.162+96G>A
ENST00000506853.5:n.541+96G>A
ENST00000510635.1:c.203+96G>A
ENST00000510955.5:n.428+96G>A
NM_000027.3:c.507+96G>A NP_000018.2:n.507+96G>A
NM_001171988.1:c.507+96G>A NP_001165459.1:n.507+96G>A
NR_033655.1:n.635+96G>A
XM_006714123.2:c.507+96G>A XP_006714186.1:n.507+96G>A
XR_001741155.2:n.601+96G>A
NM_000027.4:c.507+96G>A MANE Select NP_000018.2:n.507+96G>A
NM_001171988.2:c.507+96G>A NP_001165459.1:n.507+96G>A
NR_033655.2:n.569+96G>A