Canonical Allele Identifier: CA358783531

Gene: AGA

Linked Data

• gnomAD v4: 4-177439584-C-T
• MyVariant Identifiers: chr4:g.178360738C>T (hg19) ; chr4:g.177439584C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439584C>T , CM000666.2:g.177439584C>T	GRCh38
NC_000004.11:g.178360738C>T , CM000666.1:g.178360738C>T	GRCh37
NC_000004.10:g.178597732C>T	NCBI36
NG_011845.2:g.7920G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.386G>A MANE Select	ENSP00000264595.2:p.Gly129Glu
ENST00000264595.6:c.386G>A	ENSP00000264595.2:p.Gly129Glu
ENST00000502310.5:c.41G>A	ENSP00000423798.1:p.Gly14Glu
ENST00000506853.5:n.420G>A
ENST00000510635.1:c.82G>A
ENST00000510955.5:n.315+689G>A
NM_000027.3:c.386G>A	NP_000018.2:p.Gly129Glu
NM_001171988.1:c.386G>A	NP_001165459.1:p.Gly129Glu
NR_033655.1:n.514G>A
XM_006714123.2:c.386G>A	XP_006714186.1:p.Gly129Glu
XR_001741155.2:n.480G>A
NM_000027.4:c.386G>A MANE Select	NP_000018.2:p.Gly129Glu
NM_001171988.2:c.386G>A	NP_001165459.1:p.Gly129Glu
NR_033655.2:n.448G>A