Canonical Allele Identifier: CA2578238558
Gene: AGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439774G>A , CM000666.2:g.177439774G>A GRCh38
NC_000004.11:g.178360928G>A , CM000666.1:g.178360928G>A GRCh37
NC_000004.10:g.178597922G>A NCBI36
NG_011845.2:g.7730C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.282-86C>T MANE Select ENSP00000264595.2:n.282-86C>T
ENST00000264595.6:c.282-86C>T ENSP00000264595.2:n.282-86C>T
ENST00000506853.5:n.316-86C>T
ENST00000510955.5:n.315+499C>T
NM_000027.3:c.282-86C>T NP_000018.2:n.282-86C>T
NM_001171988.1:c.282-86C>T NP_001165459.1:n.282-86C>T
NR_033655.1:n.410-86C>T
XM_006714123.2:c.282-86C>T XP_006714186.1:n.282-86C>T
XR_001741155.2:n.376-86C>T
NM_000027.4:c.282-86C>T MANE Select NP_000018.2:n.282-86C>T
NM_001171988.2:c.282-86C>T NP_001165459.1:n.282-86C>T
NR_033655.2:n.344-86C>T