Canonical Allele Identifier: CA2575976784

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265402del , CM000678.2:g.31265402del	GRCh38
NC_000016.9:g.31276723del , CM000678.1:g.31276723del	GRCh37
NC_000016.8:g.31184224del	NCBI36
NG_011719.1:g.10436del

Transcript Alleles

HGVS	Amino-acid change
ENST00000544665.9:c.142del MANE Select	ENSP00000441691.3:p.Val48LeufsTer7
ENST00000648685.1:c.142del	ENSP00000496959.1:p.Val48LeufsTer7
ENST00000287497.12:c.142del	ENSP00000287497.8:p.Val48LeufsTer7
ENST00000544665.7:c.142del	ENSP00000441691.2:p.Val48LeufsTer7
NM_000632.3:c.142del	NP_000623.2:p.Val48LeufsTer7
NM_001145808.1:c.142del	NP_001139280.1:p.Val48LeufsTer7
XM_006721045.1:c.142del	XP_006721108.1:p.Val48LeufsTer7
XM_011545850.1:c.-74del	XP_011544152.1:n.-74del
XM_011545851.1:c.142del	XP_011544153.1:p.Val48LeufsTer7
XR_950796.1:n.232del
XM_011545850.2:c.-74del	XP_011544152.1:n.-74del
XM_011545851.2:c.142del	XP_011544153.1:p.Val48LeufsTer7
XM_017023216.1:c.142del	XP_016878705.1:p.Val48LeufsTer7
NM_000632.4:c.142del MANE Select	NP_000623.2:p.Val48LeufsTer7
NM_001145808.2:c.142del	NP_001139280.1:p.Val48LeufsTer7