Canonical Allele Identifier: CA358783236

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178359922T>C (hg19) ; chr4:g.177438768T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438768T>C , CM000666.2:g.177438768T>C	GRCh38
NC_000004.11:g.178359922T>C , CM000666.1:g.178359922T>C	GRCh37
NC_000004.10:g.178596916T>C	NCBI36
NG_011845.2:g.8736A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.484A>G MANE Select	ENSP00000264595.2:p.Asn162Asp
ENST00000264595.6:c.484A>G	ENSP00000264595.2:p.Asn162Asp
ENST00000502310.5:c.139A>G	ENSP00000423798.1:p.Asn47Asp
ENST00000506853.5:n.518A>G
ENST00000510635.1:c.180A>G
ENST00000510955.5:n.405A>G
NM_000027.3:c.484A>G	NP_000018.2:p.Asn162Asp
NM_001171988.1:c.484A>G	NP_001165459.1:p.Asn162Asp
NR_033655.1:n.612A>G
XM_006714123.2:c.484A>G	XP_006714186.1:p.Asn162Asp
XR_001741155.2:n.578A>G
NM_000027.4:c.484A>G MANE Select	NP_000018.2:p.Asn162Asp
NM_001171988.2:c.484A>G	NP_001165459.1:p.Asn162Asp
NR_033655.2:n.546A>G