Canonical Allele Identifier: CA358782149

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178355566T>G (hg19) ; chr4:g.177434412T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434412T>G , CM000666.2:g.177434412T>G	GRCh38
NC_000004.11:g.178355566T>G , CM000666.1:g.178355566T>G	GRCh37
NC_000004.10:g.178592560T>G	NCBI36
NG_011845.2:g.13092A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.776A>C MANE Select	ENSP00000264595.2:p.Asn259Thr
ENST00000264595.6:c.776A>C	ENSP00000264595.2:p.Asn259Thr
ENST00000502310.5:c.347A>C	ENSP00000423798.1:p.Asn116Thr
ENST00000506853.5:n.734A>C
NM_000027.3:c.776A>C	NP_000018.2:p.Asn259Thr
NM_001171988.1:c.746A>C	NP_001165459.1:p.Asn249Thr
NR_033655.1:n.828A>C
XM_006714123.2:c.*70A>C	XP_006714186.1:n.*70A>C
XR_001741155.2:n.848A>C
NM_000027.4:c.776A>C MANE Select	NP_000018.2:p.Asn259Thr
NM_001171988.2:c.746A>C	NP_001165459.1:p.Asn249Thr
NR_033655.2:n.762A>C