Canonical Allele Identifier: CA1515648802
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442148T= , CM000666.2:g.177442148T= GRCh38
NC_000004.11:g.178363302T= , CM000666.1:g.178363302T= GRCh37
NC_000004.10:g.178600296T= NCBI36
NG_011845.2:g.5356A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.127+101A= MANE Select ENSP00000264595.2:n.127+101A=
ENST00000264595.6:c.127+101A= ENSP00000264595.2:n.127+101A=
ENST00000506853.5:n.161+101A=
ENST00000510955.5:n.161+101A=
ENST00000511231.1:n.161+101A=
NM_000027.3:c.127+101A= NP_000018.2:n.127+101A=
NM_001171988.1:c.127+101A= NP_001165459.1:n.127+101A=
NR_033655.1:n.255+101A=
XM_006714123.2:c.127+101A= XP_006714186.1:n.127+101A=
XR_001741155.2:n.221+101A=
NM_000027.4:c.127+101A= MANE Select NP_000018.2:n.127+101A=
NM_001171988.2:c.127+101A= NP_001165459.1:n.127+101A=
NR_033655.2:n.189+101A=