Canonical Allele Identifier: CA1515649786
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442410C= , CM000666.2:g.177442410C= GRCh38
NC_000004.11:g.178363564C= , CM000666.1:g.178363564C= GRCh37
NC_000004.10:g.178600558C= NCBI36
NG_011845.2:g.5094G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-35G= MANE Select ENSP00000264595.2:n.-35G=
ENST00000264595.6:c.-35G= ENSP00000264595.2:n.-35G=
NM_000027.3:c.-35G= NP_000018.2:n.-35G=
NM_001171988.1:c.-35G= NP_001165459.1:n.-35G=
NR_033655.1:n.94G=
XM_006714123.2:c.-35G= XP_006714186.1:n.-35G=
XR_001741155.2:n.60G=
NM_000027.4:c.-35G= MANE Select NP_000018.2:n.-35G=
NM_001171988.2:c.-35G= NP_001165459.1:n.-35G=
NR_033655.2:n.28G=