Canonical Allele Identifier: CA1515649863
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442427G= , CM000666.2:g.177442427G= GRCh38
NC_000004.11:g.178363581G= , CM000666.1:g.178363581G= GRCh37
NC_000004.10:g.178600575G= NCBI36
NG_011845.2:g.5077C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-52C= MANE Select ENSP00000264595.2:n.-52C=
ENST00000264595.6:c.-52C= ENSP00000264595.2:n.-52C=
NM_000027.3:c.-52C= NP_000018.2:n.-52C=
NM_001171988.1:c.-52C= NP_001165459.1:n.-52C=
NR_033655.1:n.77C=
XM_006714123.2:c.-52C= XP_006714186.1:n.-52C=
XR_001741155.2:n.43C=
NM_000027.4:c.-52C= MANE Select NP_000018.2:n.-52C=
NM_001171988.2:c.-52C= NP_001165459.1:n.-52C=
NR_033655.2:n.11C=