Canonical Allele Identifier: CA2764653745
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437603G>C , CM000666.2:g.177437603G>C GRCh38
NC_000004.11:g.178358757G>C , CM000666.1:g.178358757G>C GRCh37
NC_000004.10:g.178595751G>C NCBI36
NG_011845.2:g.9901C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.508-84C>G MANE Select ENSP00000264595.2:n.508-84C>G
ENST00000264595.6:c.508-84C>G ENSP00000264595.2:n.508-84C>G
ENST00000502310.5:c.163-84C>G ENSP00000423798.1:n.163-84C>G
ENST00000506853.5:n.542-84C>G
ENST00000510635.1:c.204-84C>G
ENST00000510955.5:n.429-84C>G
NM_000027.3:c.508-84C>G NP_000018.2:n.508-84C>G
NM_001171988.1:c.508-84C>G NP_001165459.1:n.508-84C>G
NR_033655.1:n.636-84C>G
XM_006714123.2:c.508-84C>G XP_006714186.1:n.508-84C>G
XR_001741155.2:n.602-84C>G
NM_000027.4:c.508-84C>G MANE Select NP_000018.2:n.508-84C>G
NM_001171988.2:c.508-84C>G NP_001165459.1:n.508-84C>G
NR_033655.2:n.570-84C>G