Canonical Allele Identifier: CA358785020

Gene: AGA

Linked Data

• gnomAD v4: 4-177442268-A-T
• MyVariant Identifiers: chr4:g.178363422A>T (hg19) ; chr4:g.177442268A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442268A>T , CM000666.2:g.177442268A>T	GRCh38
NC_000004.11:g.178363422A>T , CM000666.1:g.178363422A>T	GRCh37
NC_000004.10:g.178600416A>T	NCBI36
NG_011845.2:g.5236T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.108T>A MANE Select	ENSP00000264595.2:p.Phe36Leu
ENST00000264595.6:c.108T>A	ENSP00000264595.2:p.Phe36Leu
ENST00000506853.5:n.142T>A
ENST00000510955.5:n.142T>A
ENST00000511231.1:n.142T>A
NM_000027.3:c.108T>A	NP_000018.2:p.Phe36Leu
NM_001171988.1:c.108T>A	NP_001165459.1:p.Phe36Leu
NR_033655.1:n.236T>A
XM_006714123.2:c.108T>A	XP_006714186.1:p.Phe36Leu
XR_001741155.2:n.202T>A
NM_000027.4:c.108T>A MANE Select	NP_000018.2:p.Phe36Leu
NM_001171988.2:c.108T>A	NP_001165459.1:p.Phe36Leu
NR_033655.2:n.170T>A