Canonical Allele Identifier: CA442332299

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178355589T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434435T>A , CM000666.2:g.177434435T>A	GRCh38
NC_000004.11:g.178355589T>A , CM000666.1:g.178355589T>A	GRCh37
NC_000004.10:g.178592583T>A	NCBI36
NG_011845.2:g.13069A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.753A>T MANE Select	ENSP00000264595.2:p.Ala251=
ENST00000264595.6:c.753A>T	ENSP00000264595.2:p.Ala251=
ENST00000502310.5:c.324A>T	ENSP00000423798.1:p.Ala108=
ENST00000506853.5:n.711A>T
NM_000027.3:c.753A>T	NP_000018.2:p.Ala251=
NM_001171988.1:c.723A>T	NP_001165459.1:p.Ala241=
NR_033655.1:n.805A>T
XM_006714123.2:c.*47A>T	XP_006714186.1:n.*47A>T
XR_001741155.2:n.825A>T
NM_000027.4:c.753A>T MANE Select	NP_000018.2:p.Ala251=
NM_001171988.2:c.723A>T	NP_001165459.1:p.Ala241=
NR_033655.2:n.739A>T