Canonical Allele Identifier: CA2672746422

Gene: AGA

Linked Data

• gnomAD v4: 4-177434568-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434568A>T , CM000666.2:g.177434568A>T	GRCh38
NC_000004.11:g.178355722A>T , CM000666.1:g.178355722A>T	GRCh37
NC_000004.10:g.178592716A>T	NCBI36
NG_011845.2:g.12936T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.699-79T>A MANE Select	ENSP00000264595.2:n.699-79T>A
ENST00000264595.6:c.699-79T>A	ENSP00000264595.2:n.699-79T>A
ENST00000502310.5:c.278-87T>A	ENSP00000423798.1:n.278-87T>A
ENST00000506853.5:n.657-79T>A
ENST00000510635.1:c.373-87T>A
NM_000027.3:c.699-79T>A	NP_000018.2:n.699-79T>A
NM_001171988.1:c.677-87T>A	NP_001165459.1:n.677-87T>A
NR_033655.1:n.751-79T>A
XM_006714123.2:c.677-79T>A	XP_006714186.1:n.677-79T>A
XR_001741155.2:n.771-79T>A
NM_000027.4:c.699-79T>A MANE Select	NP_000018.2:n.699-79T>A
NM_001171988.2:c.677-87T>A	NP_001165459.1:n.677-87T>A
NR_033655.2:n.685-79T>A