Canonical Allele Identifier: CA1515643541

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438806G= , CM000666.2:g.177438806G=	GRCh38
NC_000004.11:g.178359960G= , CM000666.1:g.178359960G=	GRCh37
NC_000004.10:g.178596954G=	NCBI36
NG_011845.2:g.8698C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.446C= MANE Select	ENSP00000264595.2:p.Thr149=
ENST00000264595.6:c.446C=	ENSP00000264595.2:p.Thr149=
ENST00000502310.5:c.101C=	ENSP00000423798.1:p.Thr34=
ENST00000506853.5:n.480C=
ENST00000510635.1:c.142C=
ENST00000510955.5:n.367C=
NM_000027.3:c.446C=	NP_000018.2:p.Thr149=
NM_001171988.1:c.446C=	NP_001165459.1:p.Thr149=
NR_033655.1:n.574C=
XM_006714123.2:c.446C=	XP_006714186.1:p.Thr149=
XR_001741155.2:n.540C=
NM_000027.4:c.446C= MANE Select	NP_000018.2:p.Thr149=
NM_001171988.2:c.446C=	NP_001165459.1:p.Thr149=
NR_033655.2:n.508C=