Canonical Allele Identifier: CA976367490
Gene: ITGAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31322729_31322733del , CM000678.2:g.31322729_31322733del GRCh38
NC_000016.9:g.31334050_31334054del , CM000678.1:g.31334050_31334054del GRCh37
NC_000016.8:g.31241551_31241555del NCBI36
NG_011719.1:g.67763_67767del

Transcript Alleles

HGVS Amino-acid change
ENST00000544665.9:c.2002+1102_2002+1106del MANE Select ENSP00000441691.3:n.2002+1102_2002+1106del
ENST00000648685.1:c.2005+1102_2005+1106del ENSP00000496959.1:n.2005+1102_2005+1106del
ENST00000287497.12:c.2002+1102_2002+1106del ENSP00000287497.8:n.2002+1102_2002+1106del
ENST00000544665.7:c.2005+1102_2005+1106del ENSP00000441691.2:n.2005+1102_2005+1106del
ENST00000567031.1:c.454-1670_454-1666del
NM_000632.3:c.2002+1102_2002+1106del NP_000623.2:n.2002+1102_2002+1106del
NM_001145808.1:c.2005+1102_2005+1106del NP_001139280.1:n.2005+1102_2005+1106del
XM_011545850.1:c.1819+1102_1819+1106del XP_011544152.1:n.1819+1102_1819+1106del
XM_011545851.1:c.1841+1358_1841+1362del XP_011544153.1:n.1841+1358_1841+1362del
XR_950796.1:n.2095+1102_2095+1106del
XM_011545850.2:c.1819+1102_1819+1106del XP_011544152.1:n.1819+1102_1819+1106del
XM_011545851.2:c.1841+1358_1841+1362del XP_011544153.1:n.1841+1358_1841+1362del
XM_017023216.1:c.2005+1102_2005+1106del XP_016878705.1:n.2005+1102_2005+1106del
NM_000632.4:c.2002+1102_2002+1106del MANE Select NP_000623.2:n.2002+1102_2002+1106del
NM_001145808.2:c.2005+1102_2005+1106del NP_001139280.1:n.2005+1102_2005+1106del