Canonical Allele Identifier: CA2672747460

Gene: AGA

Linked Data

• gnomAD v4: 4-177438717-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438717T>A , CM000666.2:g.177438717T>A	GRCh38
NC_000004.11:g.178359871T>A , CM000666.1:g.178359871T>A	GRCh37
NC_000004.10:g.178596865T>A	NCBI36
NG_011845.2:g.8787A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.507+28A>T MANE Select	ENSP00000264595.2:n.507+28A>T
ENST00000264595.6:c.507+28A>T	ENSP00000264595.2:n.507+28A>T
ENST00000502310.5:c.162+28A>T	ENSP00000423798.1:n.162+28A>T
ENST00000506853.5:n.541+28A>T
ENST00000510635.1:c.203+28A>T
ENST00000510955.5:n.428+28A>T
NM_000027.3:c.507+28A>T	NP_000018.2:n.507+28A>T
NM_001171988.1:c.507+28A>T	NP_001165459.1:n.507+28A>T
NR_033655.1:n.635+28A>T
XM_006714123.2:c.507+28A>T	XP_006714186.1:n.507+28A>T
XR_001741155.2:n.601+28A>T
NM_000027.4:c.507+28A>T MANE Select	NP_000018.2:n.507+28A>T
NM_001171988.2:c.507+28A>T	NP_001165459.1:n.507+28A>T
NR_033655.2:n.569+28A>T