Canonical Allele Identifier: CA358782616

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178358582T>C (hg19) ; chr4:g.177437428T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437428T>C , CM000666.2:g.177437428T>C	GRCh38
NC_000004.11:g.178358582T>C , CM000666.1:g.178358582T>C	GRCh37
NC_000004.10:g.178595576T>C	NCBI36
NG_011845.2:g.10076A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.599A>G MANE Select	ENSP00000264595.2:p.Asp200Gly
ENST00000264595.6:c.599A>G	ENSP00000264595.2:p.Asp200Gly
ENST00000502310.5:c.254A>G	ENSP00000423798.1:p.Asp85Gly
ENST00000506853.5:n.633A>G
ENST00000510635.1:c.295A>G
ENST00000510955.5:n.520A>G
NM_000027.3:c.599A>G	NP_000018.2:p.Asp200Gly
NM_001171988.1:c.599A>G	NP_001165459.1:p.Asp200Gly
NR_033655.1:n.727A>G
XM_006714123.2:c.599A>G	XP_006714186.1:p.Asp200Gly
XR_001741155.2:n.693A>G
NM_000027.4:c.599A>G MANE Select	NP_000018.2:p.Asp200Gly
NM_001171988.2:c.599A>G	NP_001165459.1:p.Asp200Gly
NR_033655.2:n.661A>G