Canonical Allele Identifier: CA2594018430
Gene: ITGAM HGNC NCBI

Linked Data

dbSNP Id: rs2144257439

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31265333del , CM000678.2:g.31265333del GRCh38
NC_000016.9:g.31276654del , CM000678.1:g.31276654del GRCh37
NC_000016.8:g.31184155del NCBI36
NG_011719.1:g.10367del

Transcript Alleles

HGVS Amino-acid change
ENST00000544665.9:c.135-62del MANE Select ENSP00000441691.3:n.135-62del
ENST00000648685.1:c.135-62del ENSP00000496959.1:n.135-62del
ENST00000287497.12:c.135-62del ENSP00000287497.8:n.135-62del
ENST00000544665.7:c.135-62del ENSP00000441691.2:n.135-62del
NM_000632.3:c.135-62del NP_000623.2:n.135-62del
NM_001145808.1:c.135-62del NP_001139280.1:n.135-62del
XM_006721045.1:c.135-62del XP_006721108.1:n.135-62del
XM_011545851.1:c.135-62del XP_011544153.1:n.135-62del
XR_950796.1:n.225-62del
XM_011545851.2:c.135-62del XP_011544153.1:n.135-62del
XM_017023216.1:c.135-62del XP_016878705.1:n.135-62del
NM_000632.4:c.135-62del MANE Select NP_000623.2:n.135-62del
NM_001145808.2:c.135-62del NP_001139280.1:n.135-62del