Canonical Allele Identifier: CA1515644854
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177439646A= , CM000666.2:g.177439646A= GRCh38
NC_000004.11:g.178360800A= , CM000666.1:g.178360800A= GRCh37
NC_000004.10:g.178597794A= NCBI36
NG_011845.2:g.7858T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.324T= MANE Select ENSP00000264595.2:p.Ile108=
ENST00000264595.6:c.324T= ENSP00000264595.2:p.Ile108=
ENST00000506853.5:n.358T=
ENST00000510635.1:c.20T=
ENST00000510955.5:n.315+627T=
NM_000027.3:c.324T= NP_000018.2:p.Ile108=
NM_001171988.1:c.324T= NP_001165459.1:p.Ile108=
NR_033655.1:n.452T=
XM_006714123.2:c.324T= XP_006714186.1:p.Ile108=
XR_001741155.2:n.418T=
NM_000027.4:c.324T= MANE Select NP_000018.2:p.Ile108=
NM_001171988.2:c.324T= NP_001165459.1:p.Ile108=
NR_033655.2:n.386T=