Canonical Allele Identifier: CA358782814

Gene: AGA

Linked Data

• gnomAD v4: 4-177437470-C-T
• MyVariant Identifiers: chr4:g.178358624C>T (hg19) ; chr4:g.177437470C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437470C>T , CM000666.2:g.177437470C>T	GRCh38
NC_000004.11:g.178358624C>T , CM000666.1:g.178358624C>T	GRCh37
NC_000004.10:g.178595618C>T	NCBI36
NG_011845.2:g.10034G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.557G>A MANE Select	ENSP00000264595.2:p.Gly186Asp
ENST00000264595.6:c.557G>A	ENSP00000264595.2:p.Gly186Asp
ENST00000502310.5:c.212G>A	ENSP00000423798.1:p.Gly71Asp
ENST00000506853.5:n.591G>A
ENST00000510635.1:c.253G>A
ENST00000510955.5:n.478G>A
NM_000027.3:c.557G>A	NP_000018.2:p.Gly186Asp
NM_001171988.1:c.557G>A	NP_001165459.1:p.Gly186Asp
NR_033655.1:n.685G>A
XM_006714123.2:c.557G>A	XP_006714186.1:p.Gly186Asp
XR_001741155.2:n.651G>A
NM_000027.4:c.557G>A MANE Select	NP_000018.2:p.Gly186Asp
NM_001171988.2:c.557G>A	NP_001165459.1:p.Gly186Asp
NR_033655.2:n.619G>A