Canonical Allele Identifier: CA358782630

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178358585T>C (hg19) ; chr4:g.177437431T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437431T>C , CM000666.2:g.177437431T>C	GRCh38
NC_000004.11:g.178358585T>C , CM000666.1:g.178358585T>C	GRCh37
NC_000004.10:g.178595579T>C	NCBI36
NG_011845.2:g.10073A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.596A>G MANE Select	ENSP00000264595.2:p.Glu199Gly
ENST00000264595.6:c.596A>G	ENSP00000264595.2:p.Glu199Gly
ENST00000502310.5:c.251A>G	ENSP00000423798.1:p.Glu84Gly
ENST00000506853.5:n.630A>G
ENST00000510635.1:c.292A>G
ENST00000510955.5:n.517A>G
NM_000027.3:c.596A>G	NP_000018.2:p.Glu199Gly
NM_001171988.1:c.596A>G	NP_001165459.1:p.Glu199Gly
NR_033655.1:n.724A>G
XM_006714123.2:c.596A>G	XP_006714186.1:p.Glu199Gly
XR_001741155.2:n.690A>G
NM_000027.4:c.596A>G MANE Select	NP_000018.2:p.Glu199Gly
NM_001171988.2:c.596A>G	NP_001165459.1:p.Glu199Gly
NR_033655.2:n.658A>G