Canonical Allele Identifier: CA1515649743
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442394C= , CM000666.2:g.177442394C= GRCh38
NC_000004.11:g.178363548C= , CM000666.1:g.178363548C= GRCh37
NC_000004.10:g.178600542C= NCBI36
NG_011845.2:g.5110G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-19G= MANE Select ENSP00000264595.2:n.-19G=
ENST00000264595.6:c.-19G= ENSP00000264595.2:n.-19G=
ENST00000506853.5:n.16G=
ENST00000510955.5:n.16G=
ENST00000511231.1:n.16G=
NM_000027.3:c.-19G= NP_000018.2:n.-19G=
NM_001171988.1:c.-19G= NP_001165459.1:n.-19G=
NR_033655.1:n.110G=
XM_006714123.2:c.-19G= XP_006714186.1:n.-19G=
XR_001741155.2:n.76G=
NM_000027.4:c.-19G= MANE Select NP_000018.2:n.-19G=
NM_001171988.2:c.-19G= NP_001165459.1:n.-19G=
NR_033655.2:n.44G=