Canonical Allele Identifier: CA395714061
Gene: ITGAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31363372C>G , CM000678.2:g.31363372C>G GRCh38
NC_000016.9:g.31374693C>G , CM000678.1:g.31374693C>G GRCh37
NC_000016.8:g.31282194C>G NCBI36
NG_011451.1:g.13185C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000268296.9:c.1708C>G MANE Select ENSP00000268296.5:p.Gln570Glu
ENST00000268296.8:c.1708C>G ENSP00000268296.4:p.Gln570Glu
ENST00000562522.2:c.1708C>G ENSP00000454623.1:p.Gln570Glu
ENST00000571644.1:n.1729C>G
NM_000887.4:c.1708C>G NP_000878.2:p.Gln570Glu
NM_001286375.1:c.1708C>G NP_001273304.1:p.Gln570Glu
XM_011545852.1:c.1708C>G XP_011544154.1:p.Gln570Glu
XM_011545853.1:c.1708C>G XP_011544155.1:p.Gln570Glu
XM_011545854.1:c.1708C>G XP_011544156.1:p.Gln570Glu
XR_950797.1:n.1796C>G
XM_024450263.1:c.658C>G XP_024306031.1:p.Gln220Glu
XR_950797.2:n.1796C>G
NM_000887.5:c.1708C>G MANE Select NP_000878.2:p.Gln570Glu
NM_001286375.2:c.1708C>G NP_001273304.1:p.Gln570Glu