Canonical Allele Identifier: CA358782209
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434424G>T , CM000666.2:g.177434424G>T GRCh38
NC_000004.11:g.178355578G>T , CM000666.1:g.178355578G>T GRCh37
NC_000004.10:g.178592572G>T NCBI36
NG_011845.2:g.13080C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.764C>A MANE Select ENSP00000264595.2:p.Ala255Glu
ENST00000264595.6:c.764C>A ENSP00000264595.2:p.Ala255Glu
ENST00000502310.5:c.335C>A ENSP00000423798.1:p.Ala112Glu
ENST00000506853.5:n.722C>A
NM_000027.3:c.764C>A NP_000018.2:p.Ala255Glu
NM_001171988.1:c.734C>A NP_001165459.1:p.Ala245Glu
NR_033655.1:n.816C>A
XM_006714123.2:c.*58C>A XP_006714186.1:n.*58C>A
XR_001741155.2:n.836C>A
NM_000027.4:c.764C>A MANE Select NP_000018.2:p.Ala255Glu
NM_001171988.2:c.734C>A NP_001165459.1:p.Ala245Glu
NR_033655.2:n.750C>A