Canonical Allele Identifier: CA1515637810
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434503T= , CM000666.2:g.177434503T= GRCh38
NC_000004.11:g.178355657T= , CM000666.1:g.178355657T= GRCh37
NC_000004.10:g.178592651T= NCBI36
NG_011845.2:g.13001A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.699-14A= MANE Select ENSP00000264595.2:n.699-14A=
ENST00000264595.6:c.699-14A= ENSP00000264595.2:n.699-14A=
ENST00000502310.5:c.278-22A= ENSP00000423798.1:n.278-22A=
ENST00000506853.5:n.657-14A=
ENST00000510635.1:c.373-22A=
NM_000027.3:c.699-14A= NP_000018.2:n.699-14A=
NM_001171988.1:c.677-22A= NP_001165459.1:n.677-22A=
NR_033655.1:n.751-14A=
XM_006714123.2:c.677-14A= XP_006714186.1:n.677-14A=
XR_001741155.2:n.771-14A=
NM_000027.4:c.699-14A= MANE Select NP_000018.2:n.699-14A=
NM_001171988.2:c.677-22A= NP_001165459.1:n.677-22A=
NR_033655.2:n.685-14A=