Canonical Allele Identifier: CA976367493
Gene: ITGAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31322735_31322736insAAAAA , CM000678.2:g.31322735_31322736insAAAAA GRCh38
NC_000016.9:g.31334056_31334057insAAAAA , CM000678.1:g.31334056_31334057insAAAAA GRCh37
NC_000016.8:g.31241557_31241558insAAAAA NCBI36
NG_011719.1:g.67769_67770insAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000544665.9:c.2002+1108_2002+1109insAAAAA MANE Select ENSP00000441691.3:n.2002+1108_2002+1109insAAAAA
ENST00000648685.1:c.2005+1108_2005+1109insAAAAA ENSP00000496959.1:n.2005+1108_2005+1109insAAAAA
ENST00000287497.12:c.2002+1108_2002+1109insAAAAA ENSP00000287497.8:n.2002+1108_2002+1109insAAAAA
ENST00000544665.7:c.2005+1108_2005+1109insAAAAA ENSP00000441691.2:n.2005+1108_2005+1109insAAAAA
ENST00000567031.1:c.454-1664_454-1663insAAAAA
NM_000632.3:c.2002+1108_2002+1109insAAAAA NP_000623.2:n.2002+1108_2002+1109insAAAAA
NM_001145808.1:c.2005+1108_2005+1109insAAAAA NP_001139280.1:n.2005+1108_2005+1109insAAAAA
XM_011545850.1:c.1819+1108_1819+1109insAAAAA XP_011544152.1:n.1819+1108_1819+1109insAAAAA
XM_011545851.1:c.1841+1364_1841+1365insAAAAA XP_011544153.1:n.1841+1364_1841+1365insAAAAA
XR_950796.1:n.2095+1108_2095+1109insAAAAA
XM_011545850.2:c.1819+1108_1819+1109insAAAAA XP_011544152.1:n.1819+1108_1819+1109insAAAAA
XM_011545851.2:c.1841+1364_1841+1365insAAAAA XP_011544153.1:n.1841+1364_1841+1365insAAAAA
XM_017023216.1:c.2005+1108_2005+1109insAAAAA XP_016878705.1:n.2005+1108_2005+1109insAAAAA
NM_000632.4:c.2002+1108_2002+1109insAAAAA MANE Select NP_000623.2:n.2002+1108_2002+1109insAAAAA
NM_001145808.2:c.2005+1108_2005+1109insAAAAA NP_001139280.1:n.2005+1108_2005+1109insAAAAA