Canonical Allele Identifier: CA358783707
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439640A>C , CM000666.2:g.177439640A>C GRCh38
NC_000004.11:g.178360794A>C , CM000666.1:g.178360794A>C GRCh37
NC_000004.10:g.178597788A>C NCBI36
NG_011845.2:g.7864T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.330T>G MANE Select ENSP00000264595.2:p.Asn110Lys
ENST00000264595.6:c.330T>G ENSP00000264595.2:p.Asn110Lys
ENST00000506853.5:n.364T>G
ENST00000510635.1:c.26T>G
ENST00000510955.5:n.315+633T>G
NM_000027.3:c.330T>G NP_000018.2:p.Asn110Lys
NM_001171988.1:c.330T>G NP_001165459.1:p.Asn110Lys
NR_033655.1:n.458T>G
XM_006714123.2:c.330T>G XP_006714186.1:p.Asn110Lys
XR_001741155.2:n.424T>G
NM_000027.4:c.330T>G MANE Select NP_000018.2:p.Asn110Lys
NM_001171988.2:c.330T>G NP_001165459.1:p.Asn110Lys
NR_033655.2:n.392T>G