Canonical Allele Identifier: CA2672747248

Gene: AGA

Linked Data

• gnomAD v4: 4-177437627-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437627G>A , CM000666.2:g.177437627G>A	GRCh38
NC_000004.11:g.178358781G>A , CM000666.1:g.178358781G>A	GRCh37
NC_000004.10:g.178595775G>A	NCBI36
NG_011845.2:g.9877C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.508-108C>T MANE Select	ENSP00000264595.2:n.508-108C>T
ENST00000264595.6:c.508-108C>T	ENSP00000264595.2:n.508-108C>T
ENST00000502310.5:c.163-108C>T	ENSP00000423798.1:n.163-108C>T
ENST00000506853.5:n.542-108C>T
ENST00000510635.1:c.204-108C>T
ENST00000510955.5:n.429-108C>T
NM_000027.3:c.508-108C>T	NP_000018.2:n.508-108C>T
NM_001171988.1:c.508-108C>T	NP_001165459.1:n.508-108C>T
NR_033655.1:n.636-108C>T
XM_006714123.2:c.508-108C>T	XP_006714186.1:n.508-108C>T
XR_001741155.2:n.602-108C>T
NM_000027.4:c.508-108C>T MANE Select	NP_000018.2:n.508-108C>T
NM_001171988.2:c.508-108C>T	NP_001165459.1:n.508-108C>T
NR_033655.2:n.570-108C>T