Canonical Allele Identifier: CA2672747988

Gene: AGA

Linked Data

• gnomAD v4: 4-177439732-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439732A>T , CM000666.2:g.177439732A>T	GRCh38
NC_000004.11:g.178360886A>T , CM000666.1:g.178360886A>T	GRCh37
NC_000004.10:g.178597880A>T	NCBI36
NG_011845.2:g.7772T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.282-44T>A MANE Select	ENSP00000264595.2:n.282-44T>A
ENST00000264595.6:c.282-44T>A	ENSP00000264595.2:n.282-44T>A
ENST00000506853.5:n.316-44T>A
ENST00000510955.5:n.315+541T>A
NM_000027.3:c.282-44T>A	NP_000018.2:n.282-44T>A
NM_001171988.1:c.282-44T>A	NP_001165459.1:n.282-44T>A
NR_033655.1:n.410-44T>A
XM_006714123.2:c.282-44T>A	XP_006714186.1:n.282-44T>A
XR_001741155.2:n.376-44T>A
NM_000027.4:c.282-44T>A MANE Select	NP_000018.2:n.282-44T>A
NM_001171988.2:c.282-44T>A	NP_001165459.1:n.282-44T>A
NR_033655.2:n.344-44T>A