Canonical Allele Identifier: CA2672748516

Gene: AGA

Linked Data

• gnomAD v4: 4-177442157-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442157C>G , CM000666.2:g.177442157C>G	GRCh38
NC_000004.11:g.178363311C>G , CM000666.1:g.178363311C>G	GRCh37
NC_000004.10:g.178600305C>G	NCBI36
NG_011845.2:g.5347G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.127+92G>C MANE Select	ENSP00000264595.2:n.127+92G>C
ENST00000264595.6:c.127+92G>C	ENSP00000264595.2:n.127+92G>C
ENST00000506853.5:n.161+92G>C
ENST00000510955.5:n.161+92G>C
ENST00000511231.1:n.161+92G>C
NM_000027.3:c.127+92G>C	NP_000018.2:n.127+92G>C
NM_001171988.1:c.127+92G>C	NP_001165459.1:n.127+92G>C
NR_033655.1:n.255+92G>C
XM_006714123.2:c.127+92G>C	XP_006714186.1:n.127+92G>C
XR_001741155.2:n.221+92G>C
NM_000027.4:c.127+92G>C MANE Select	NP_000018.2:n.127+92G>C
NM_001171988.2:c.127+92G>C	NP_001165459.1:n.127+92G>C
NR_033655.2:n.189+92G>C