Canonical Allele Identifier: CA442332338

Gene: AGA

Linked Data

• gnomAD v4: 4-177434489-G-T
• MyVariant Identifiers: chr4:g.178355643G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434489G>T , CM000666.2:g.177434489G>T	GRCh38
NC_000004.11:g.178355643G>T , CM000666.1:g.178355643G>T	GRCh37
NC_000004.10:g.178592637G>T	NCBI36
NG_011845.2:g.13015C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.699C>A MANE Select	ENSP00000264595.2:p.Gly233=
ENST00000264595.6:c.699C>A	ENSP00000264595.2:p.Gly233=
ENST00000502310.5:c.278-8C>A	ENSP00000423798.1:n.278-8C>A
ENST00000506853.5:n.657C>A
ENST00000510635.1:c.373-8C>A
NM_000027.3:c.699C>A	NP_000018.2:p.Gly233=
NM_001171988.1:c.677-8C>A	NP_001165459.1:n.677-8C>A
NR_033655.1:n.751C>A
XM_006714123.2:c.677C>A	XP_006714186.1:p.Ala226Asp
XR_001741155.2:n.771C>A
NM_000027.4:c.699C>A MANE Select	NP_000018.2:p.Gly233=
NM_001171988.2:c.677-8C>A	NP_001165459.1:n.677-8C>A
NR_033655.2:n.685C>A