Canonical Allele Identifier: CA1515645027
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439710T= , CM000666.2:g.177439710T= GRCh38
NC_000004.11:g.178360864T= , CM000666.1:g.178360864T= GRCh37
NC_000004.10:g.178597858T= NCBI36
NG_011845.2:g.7794A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.282-22A= MANE Select ENSP00000264595.2:n.282-22A=
ENST00000264595.6:c.282-22A= ENSP00000264595.2:n.282-22A=
ENST00000506853.5:n.316-22A=
ENST00000510955.5:n.315+563A=
NM_000027.3:c.282-22A= NP_000018.2:n.282-22A=
NM_001171988.1:c.282-22A= NP_001165459.1:n.282-22A=
NR_033655.1:n.410-22A=
XM_006714123.2:c.282-22A= XP_006714186.1:n.282-22A=
XR_001741155.2:n.376-22A=
NM_000027.4:c.282-22A= MANE Select NP_000018.2:n.282-22A=
NM_001171988.2:c.282-22A= NP_001165459.1:n.282-22A=
NR_033655.2:n.344-22A=