Canonical Allele Identifier: CA1515649801
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442413G= , CM000666.2:g.177442413G= GRCh38
NC_000004.11:g.178363567G= , CM000666.1:g.178363567G= GRCh37
NC_000004.10:g.178600561G= NCBI36
NG_011845.2:g.5091C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-38C= MANE Select ENSP00000264595.2:n.-38C=
ENST00000264595.6:c.-38C= ENSP00000264595.2:n.-38C=
NM_000027.3:c.-38C= NP_000018.2:n.-38C=
NM_001171988.1:c.-38C= NP_001165459.1:n.-38C=
NR_033655.1:n.91C=
XM_006714123.2:c.-38C= XP_006714186.1:n.-38C=
XR_001741155.2:n.57C=
NM_000027.4:c.-38C= MANE Select NP_000018.2:n.-38C=
NM_001171988.2:c.-38C= NP_001165459.1:n.-38C=
NR_033655.2:n.25C=