Canonical Allele Identifier: CA2578238416
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434552C>G , CM000666.2:g.177434552C>G GRCh38
NC_000004.11:g.178355706C>G , CM000666.1:g.178355706C>G GRCh37
NC_000004.10:g.178592700C>G NCBI36
NG_011845.2:g.12952G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.699-63G>C MANE Select ENSP00000264595.2:n.699-63G>C
ENST00000264595.6:c.699-63G>C ENSP00000264595.2:n.699-63G>C
ENST00000502310.5:c.278-71G>C ENSP00000423798.1:n.278-71G>C
ENST00000506853.5:n.657-63G>C
ENST00000510635.1:c.373-71G>C
NM_000027.3:c.699-63G>C NP_000018.2:n.699-63G>C
NM_001171988.1:c.677-71G>C NP_001165459.1:n.677-71G>C
NR_033655.1:n.751-63G>C
XM_006714123.2:c.677-63G>C XP_006714186.1:n.677-63G>C
XR_001741155.2:n.771-63G>C
NM_000027.4:c.699-63G>C MANE Select NP_000018.2:n.699-63G>C
NM_001171988.2:c.677-71G>C NP_001165459.1:n.677-71G>C
NR_033655.2:n.685-63G>C