Canonical Allele Identifier: CA358783704
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439639C>A , CM000666.2:g.177439639C>A GRCh38
NC_000004.11:g.178360793C>A , CM000666.1:g.178360793C>A GRCh37
NC_000004.10:g.178597787C>A NCBI36
NG_011845.2:g.7865G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.331G>T MANE Select ENSP00000264595.2:p.Ala111Ser
ENST00000264595.6:c.331G>T ENSP00000264595.2:p.Ala111Ser
ENST00000506853.5:n.365G>T
ENST00000510635.1:c.27G>T
ENST00000510955.5:n.315+634G>T
NM_000027.3:c.331G>T NP_000018.2:p.Ala111Ser
NM_001171988.1:c.331G>T NP_001165459.1:p.Ala111Ser
NR_033655.1:n.459G>T
XM_006714123.2:c.331G>T XP_006714186.1:p.Ala111Ser
XR_001741155.2:n.425G>T
NM_000027.4:c.331G>T MANE Select NP_000018.2:p.Ala111Ser
NM_001171988.2:c.331G>T NP_001165459.1:p.Ala111Ser
NR_033655.2:n.393G>T