Canonical Allele Identifier: CA395716294
Gene: ITGAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31371141G>C , CM000678.2:g.31371141G>C GRCh38
NC_000016.9:g.31382462G>C , CM000678.1:g.31382462G>C GRCh37
NC_000016.8:g.31289963G>C NCBI36
NG_011451.1:g.20954G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000268296.9:c.1768G>C MANE Select ENSP00000268296.5:p.Gly590Arg
ENST00000268296.8:c.1768G>C ENSP00000268296.4:p.Gly590Arg
ENST00000562522.2:c.1768G>C ENSP00000454623.1:p.Gly590Arg
ENST00000571644.1:n.1907G>C
NM_000887.4:c.1768G>C NP_000878.2:p.Gly590Arg
NM_001286375.1:c.1768G>C NP_001273304.1:p.Gly590Arg
XM_011545852.1:c.1768G>C XP_011544154.1:p.Gly590Arg
XM_011545853.1:c.1768G>C XP_011544155.1:p.Gly590Arg
XM_011545854.1:c.1768G>C XP_011544156.1:p.Gly590Arg
XR_950797.1:n.1856G>C
XM_024450263.1:c.718G>C XP_024306031.1:p.Gly240Arg
XR_950797.2:n.1856G>C
NM_000887.5:c.1768G>C MANE Select NP_000878.2:p.Gly590Arg
NM_001286375.2:c.1768G>C NP_001273304.1:p.Gly590Arg