Canonical Allele Identifier: CA2216975860

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31322764_31322767delinsCAAA , CM000678.2:g.31322764_31322767delinsCAAA	GRCh38
NC_000016.9:g.31334085_31334088delinsCAAA , CM000678.1:g.31334085_31334088delinsCAAA	GRCh37
NC_000016.8:g.31241586_31241589delinsCAAA	NCBI36
NG_011719.1:g.67798_67801delinsCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.2002+1137_2002+1140delinsCAAA MANE Select	ENSP00000441691.3:n.2002+1137_2002+1140delinsCAAA
ENST00000648685.1:c.2005+1137_2005+1140delinsCAAA	ENSP00000496959.1:n.2005+1137_2005+1140delinsCAAA
ENST00000287497.12:c.2002+1137_2002+1140delinsCAAA	ENSP00000287497.8:n.2002+1137_2002+1140delinsCAAA
ENST00000544665.7:c.2005+1137_2005+1140delinsCAAA	ENSP00000441691.2:n.2005+1137_2005+1140delinsCAAA
ENST00000567031.1:c.454-1635_454-1632delinsCAAA
NM_000632.3:c.2002+1137_2002+1140delinsCAAA	NP_000623.2:n.2002+1137_2002+1140delinsCAAA
NM_001145808.1:c.2005+1137_2005+1140delinsCAAA	NP_001139280.1:n.2005+1137_2005+1140delinsCAAA
XM_011545850.1:c.1819+1137_1819+1140delinsCAAA	XP_011544152.1:n.1819+1137_1819+1140delinsCAAA
XM_011545851.1:c.1841+1393_1841+1396delinsCAAA	XP_011544153.1:n.1841+1393_1841+1396delinsCAAA
XR_950796.1:n.2095+1137_2095+1140delinsCAAA
XM_011545850.2:c.1819+1137_1819+1140delinsCAAA	XP_011544152.1:n.1819+1137_1819+1140delinsCAAA
XM_011545851.2:c.1841+1393_1841+1396delinsCAAA	XP_011544153.1:n.1841+1393_1841+1396delinsCAAA
XM_017023216.1:c.2005+1137_2005+1140delinsCAAA	XP_016878705.1:n.2005+1137_2005+1140delinsCAAA
NM_000632.4:c.2002+1137_2002+1140delinsCAAA MANE Select	NP_000623.2:n.2002+1137_2002+1140delinsCAAA
NM_001145808.2:c.2005+1137_2005+1140delinsCAAA	NP_001139280.1:n.2005+1137_2005+1140delinsCAAA