Canonical Allele Identifier: CA2672748526

Gene: AGA

Linked Data

• gnomAD v4: 4-177442169-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442169T>G , CM000666.2:g.177442169T>G	GRCh38
NC_000004.11:g.178363323T>G , CM000666.1:g.178363323T>G	GRCh37
NC_000004.10:g.178600317T>G	NCBI36
NG_011845.2:g.5335A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.127+80A>C MANE Select	ENSP00000264595.2:n.127+80A>C
ENST00000264595.6:c.127+80A>C	ENSP00000264595.2:n.127+80A>C
ENST00000506853.5:n.161+80A>C
ENST00000510955.5:n.161+80A>C
ENST00000511231.1:n.161+80A>C
NM_000027.3:c.127+80A>C	NP_000018.2:n.127+80A>C
NM_001171988.1:c.127+80A>C	NP_001165459.1:n.127+80A>C
NR_033655.1:n.255+80A>C
XM_006714123.2:c.127+80A>C	XP_006714186.1:n.127+80A>C
XR_001741155.2:n.221+80A>C
NM_000027.4:c.127+80A>C MANE Select	NP_000018.2:n.127+80A>C
NM_001171988.2:c.127+80A>C	NP_001165459.1:n.127+80A>C
NR_033655.2:n.189+80A>C