Canonical Allele Identifier: CA1515641660
Gene: AGA HGNC NCBI

Linked Data

dbSNP Id: rs942536079

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177437327G>A , CM000666.2:g.177437327G>A GRCh38
NC_000004.11:g.178358481G>A , CM000666.1:g.178358481G>A GRCh37
NC_000004.10:g.178595475G>A NCBI36
NG_011845.2:g.10177C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.622+78C>T MANE Select ENSP00000264595.2:n.622+78C>T
ENST00000264595.6:c.622+78C>T ENSP00000264595.2:n.622+78C>T
ENST00000502310.5:c.277+78C>T ENSP00000423798.1:n.277+78C>T
ENST00000506853.5:n.656+78C>T
ENST00000510635.1:c.318+78C>T
ENST00000510955.5:n.621C>T
NM_000027.3:c.622+78C>T NP_000018.2:n.622+78C>T
NM_001171988.1:c.622+78C>T NP_001165459.1:n.622+78C>T
NR_033655.1:n.750+78C>T
XM_006714123.2:c.622+78C>T XP_006714186.1:n.622+78C>T
XR_001741155.2:n.716+78C>T
NM_000027.4:c.622+78C>T MANE Select NP_000018.2:n.622+78C>T
NM_001171988.2:c.622+78C>T NP_001165459.1:n.622+78C>T
NR_033655.2:n.684+78C>T