Canonical Allele Identifier: CA2216975804

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31322729T= , CM000678.2:g.31322729T=	GRCh38
NC_000016.9:g.31334050T= , CM000678.1:g.31334050T=	GRCh37
NC_000016.8:g.31241551T=	NCBI36
NG_011719.1:g.67763T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.2002+1102T= MANE Select	ENSP00000441691.3:n.2002+1102T=
ENST00000648685.1:c.2005+1102T=	ENSP00000496959.1:n.2005+1102T=
ENST00000287497.12:c.2002+1102T=	ENSP00000287497.8:n.2002+1102T=
ENST00000544665.7:c.2005+1102T=	ENSP00000441691.2:n.2005+1102T=
ENST00000567031.1:c.454-1670T=
NM_000632.3:c.2002+1102T=	NP_000623.2:n.2002+1102T=
NM_001145808.1:c.2005+1102T=	NP_001139280.1:n.2005+1102T=
XM_011545850.1:c.1819+1102T=	XP_011544152.1:n.1819+1102T=
XM_011545851.1:c.1841+1358T=	XP_011544153.1:n.1841+1358T=
XR_950796.1:n.2095+1102T=
XM_011545850.2:c.1819+1102T=	XP_011544152.1:n.1819+1102T=
XM_011545851.2:c.1841+1358T=	XP_011544153.1:n.1841+1358T=
XM_017023216.1:c.2005+1102T=	XP_016878705.1:n.2005+1102T=
NM_000632.4:c.2002+1102T= MANE Select	NP_000623.2:n.2002+1102T=
NM_001145808.2:c.2005+1102T=	NP_001139280.1:n.2005+1102T=