Canonical Allele Identifier: CA2216976148

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31322995C= , CM000678.2:g.31322995C=	GRCh38
NC_000016.9:g.31334316C= , CM000678.1:g.31334316C=	GRCh37
NC_000016.8:g.31241817C=	NCBI36
NG_011719.1:g.68029C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000544665.9:c.2002+1368C= MANE Select	ENSP00000441691.3:n.2002+1368C=
ENST00000648685.1:c.2005+1368C=	ENSP00000496959.1:n.2005+1368C=
ENST00000287497.12:c.2002+1368C=	ENSP00000287497.8:n.2002+1368C=
ENST00000544665.7:c.2005+1368C=	ENSP00000441691.2:n.2005+1368C=
ENST00000567031.1:c.454-1404C=
NM_000632.3:c.2002+1368C=	NP_000623.2:n.2002+1368C=
NM_001145808.1:c.2005+1368C=	NP_001139280.1:n.2005+1368C=
XM_011545850.1:c.1819+1368C=	XP_011544152.1:n.1819+1368C=
XM_011545851.1:c.1842-1404C=	XP_011544153.1:n.1842-1404C=
XR_950796.1:n.2095+1368C=
XM_011545850.2:c.1819+1368C=	XP_011544152.1:n.1819+1368C=
XM_011545851.2:c.1842-1404C=	XP_011544153.1:n.1842-1404C=
XM_017023216.1:c.2005+1368C=	XP_016878705.1:n.2005+1368C=
NM_000632.4:c.2002+1368C= MANE Select	NP_000623.2:n.2002+1368C=
NM_001145808.2:c.2005+1368C=	NP_001139280.1:n.2005+1368C=