Canonical Allele Identifier: CA2575976783
Gene: ITGAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31265390del , CM000678.2:g.31265390del GRCh38
NC_000016.9:g.31276711del , CM000678.1:g.31276711del GRCh37
NC_000016.8:g.31184212del NCBI36
NG_011719.1:g.10424del

Transcript Alleles

HGVS Amino-acid change
ENST00000544665.9:c.135-5del MANE Select ENSP00000441691.3:n.135-5del
ENST00000648685.1:c.135-5del ENSP00000496959.1:n.135-5del
ENST00000287497.12:c.135-5del ENSP00000287497.8:n.135-5del
ENST00000544665.7:c.135-5del ENSP00000441691.2:n.135-5del
NM_000632.3:c.135-5del NP_000623.2:n.135-5del
NM_001145808.1:c.135-5del NP_001139280.1:n.135-5del
XM_006721045.1:c.135-5del XP_006721108.1:n.135-5del
XM_011545851.1:c.135-5del XP_011544153.1:n.135-5del
XR_950796.1:n.225-5del
XM_011545851.2:c.135-5del XP_011544153.1:n.135-5del
XM_017023216.1:c.135-5del XP_016878705.1:n.135-5del
NM_000632.4:c.135-5del MANE Select NP_000623.2:n.135-5del
NM_001145808.2:c.135-5del NP_001139280.1:n.135-5del