Canonical Allele Identifier: CA1515637883
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434541_177434543delinsTAA , CM000666.2:g.177434541_177434543delinsTAA GRCh38
NC_000004.11:g.178355695_178355697delinsTAA , CM000666.1:g.178355695_178355697delinsTAA GRCh37
NC_000004.10:g.178592689_178592691delinsTAA NCBI36
NG_011845.2:g.12961_12963delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.699-54_699-52delinsTTA MANE Select ENSP00000264595.2:n.699-54_699-52delinsTTA
ENST00000264595.6:c.699-54_699-52delinsTTA ENSP00000264595.2:n.699-54_699-52delinsTTA
ENST00000502310.5:c.278-62_278-60delinsTTA ENSP00000423798.1:n.278-62_278-60delinsTTA
ENST00000506853.5:n.657-54_657-52delinsTTA
ENST00000510635.1:c.373-62_373-60delinsTTA
NM_000027.3:c.699-54_699-52delinsTTA NP_000018.2:n.699-54_699-52delinsTTA
NM_001171988.1:c.677-62_677-60delinsTTA NP_001165459.1:n.677-62_677-60delinsTTA
NR_033655.1:n.751-54_751-52delinsTTA
XM_006714123.2:c.677-54_677-52delinsTTA XP_006714186.1:n.677-54_677-52delinsTTA
XR_001741155.2:n.771-54_771-52delinsTTA
NM_000027.4:c.699-54_699-52delinsTTA MANE Select NP_000018.2:n.699-54_699-52delinsTTA
NM_001171988.2:c.677-62_677-60delinsTTA NP_001165459.1:n.677-62_677-60delinsTTA
NR_033655.2:n.685-54_685-52delinsTTA