Canonical Allele Identifier: CA1515641677
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437330A= , CM000666.2:g.177437330A= GRCh38
NC_000004.11:g.178358484A= , CM000666.1:g.178358484A= GRCh37
NC_000004.10:g.178595478A= NCBI36
NG_011845.2:g.10174T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.622+75T= MANE Select ENSP00000264595.2:n.622+75T=
ENST00000264595.6:c.622+75T= ENSP00000264595.2:n.622+75T=
ENST00000502310.5:c.277+75T= ENSP00000423798.1:n.277+75T=
ENST00000506853.5:n.656+75T=
ENST00000510635.1:c.318+75T=
ENST00000510955.5:n.618T=
NM_000027.3:c.622+75T= NP_000018.2:n.622+75T=
NM_001171988.1:c.622+75T= NP_001165459.1:n.622+75T=
NR_033655.1:n.750+75T=
XM_006714123.2:c.622+75T= XP_006714186.1:n.622+75T=
XR_001741155.2:n.716+75T=
NM_000027.4:c.622+75T= MANE Select NP_000018.2:n.622+75T=
NM_001171988.2:c.622+75T= NP_001165459.1:n.622+75T=
NR_033655.2:n.684+75T=