Canonical Allele Identifier: CA2515483119
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442015G>T , CM000666.2:g.177442015G>T GRCh38
NC_000004.11:g.178363169G>T , CM000666.1:g.178363169G>T GRCh37
NC_000004.10:g.178600163G>T NCBI36
NG_011845.2:g.5489C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.127+234C>A MANE Select ENSP00000264595.2:n.127+234C>A
ENST00000264595.6:c.127+234C>A ENSP00000264595.2:n.127+234C>A
ENST00000506853.5:n.161+234C>A
ENST00000510955.5:n.161+234C>A
ENST00000511231.1:n.161+234C>A
NM_000027.3:c.127+234C>A NP_000018.2:n.127+234C>A
NM_001171988.1:c.127+234C>A NP_001165459.1:n.127+234C>A
NR_033655.1:n.255+234C>A
XM_006714123.2:c.127+234C>A XP_006714186.1:n.127+234C>A
XR_001741155.2:n.221+234C>A
NM_000027.4:c.127+234C>A MANE Select NP_000018.2:n.127+234C>A
NM_001171988.2:c.127+234C>A NP_001165459.1:n.127+234C>A
NR_033655.2:n.189+234C>A