Canonical Allele Identifier: CA1515648237

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177441857T= , CM000666.2:g.177441857T=	GRCh38
NC_000004.11:g.178363011T= , CM000666.1:g.178363011T=	GRCh37
NC_000004.10:g.178600005T=	NCBI36
NG_011845.2:g.5647A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.127+392A= MANE Select	ENSP00000264595.2:n.127+392A=
ENST00000264595.6:c.127+392A=	ENSP00000264595.2:n.127+392A=
ENST00000506853.5:n.161+392A=
ENST00000510955.5:n.161+392A=
ENST00000511231.1:n.161+392A=
NM_000027.3:c.127+392A=	NP_000018.2:n.127+392A=
NM_001171988.1:c.127+392A=	NP_001165459.1:n.127+392A=
NR_033655.1:n.255+392A=
XM_006714123.2:c.127+392A=	XP_006714186.1:n.127+392A=
XR_001741155.2:n.221+392A=
NM_000027.4:c.127+392A= MANE Select	NP_000018.2:n.127+392A=
NM_001171988.2:c.127+392A=	NP_001165459.1:n.127+392A=
NR_033655.2:n.189+392A=