Canonical Allele Identifier: CA2544924230
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434530G>A , CM000666.2:g.177434530G>A GRCh38
NC_000004.11:g.178355684G>A , CM000666.1:g.178355684G>A GRCh37
NC_000004.10:g.178592678G>A NCBI36
NG_011845.2:g.12974C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.699-41C>T MANE Select ENSP00000264595.2:n.699-41C>T
ENST00000264595.6:c.699-41C>T ENSP00000264595.2:n.699-41C>T
ENST00000502310.5:c.278-49C>T ENSP00000423798.1:n.278-49C>T
ENST00000506853.5:n.657-41C>T
ENST00000510635.1:c.373-49C>T
NM_000027.3:c.699-41C>T NP_000018.2:n.699-41C>T
NM_001171988.1:c.677-49C>T NP_001165459.1:n.677-49C>T
NR_033655.1:n.751-41C>T
XM_006714123.2:c.677-41C>T XP_006714186.1:n.677-41C>T
XR_001741155.2:n.771-41C>T
NM_000027.4:c.699-41C>T MANE Select NP_000018.2:n.699-41C>T
NM_001171988.2:c.677-49C>T NP_001165459.1:n.677-49C>T
NR_033655.2:n.685-41C>T