Canonical Allele Identifier: CA8026343
Gene: ITGAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31356669C>T , CM000678.2:g.31356669C>T GRCh38
NC_000016.9:g.31367990C>T , CM000678.1:g.31367990C>T GRCh37
NC_000016.8:g.31275491C>T NCBI36
NG_011451.1:g.6482C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000268296.9:c.188C>T MANE Select ENSP00000268296.5:p.Thr63Met
ENST00000268296.8:c.188C>T ENSP00000268296.4:p.Thr63Met
ENST00000562522.2:c.188C>T ENSP00000454623.1:p.Thr63Met
ENST00000562918.5:c.188C>T ENSP00000483860.1:p.Thr63Met
ENST00000567409.1:n.255C>T
NM_000887.4:c.188C>T NP_000878.2:p.Thr63Met
NM_001286375.1:c.188C>T NP_001273304.1:p.Thr63Met
XM_011545852.1:c.188C>T XP_011544154.1:p.Thr63Met
XM_011545853.1:c.188C>T XP_011544155.1:p.Thr63Met
XM_011545854.1:c.188C>T XP_011544156.1:p.Thr63Met
XR_950797.1:n.276C>T
XR_950797.2:n.276C>T
NM_000887.5:c.188C>T MANE Select NP_000878.2:p.Thr63Met
NM_001286375.2:c.188C>T NP_001273304.1:p.Thr63Met