Canonical Allele Identifier: CA2216992181

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265495C= , CM000678.2:g.31265495C=	GRCh38
NC_000016.9:g.31276816C= , CM000678.1:g.31276816C=	GRCh37
NC_000016.8:g.31184317C=	NCBI36
NG_011719.1:g.10529C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.235C= MANE Select	ENSP00000441691.3:p.Gln79=
ENST00000648685.1:c.235C=	ENSP00000496959.1:p.Gln79=
ENST00000287497.12:c.235C=	ENSP00000287497.8:p.Gln79=
ENST00000544665.7:c.235C=	ENSP00000441691.2:p.Gln79=
NM_000632.3:c.235C=	NP_000623.2:p.Gln79=
NM_001145808.1:c.235C=	NP_001139280.1:p.Gln79=
XM_006721045.1:c.235C=	XP_006721108.1:p.Gln79=
XM_011545850.1:c.20C=	XP_011544152.1:p.Ala7=
XM_011545851.1:c.235C=	XP_011544153.1:p.Gln79=
XR_950796.1:n.325C=
XM_011545850.2:c.20C=	XP_011544152.1:p.Ala7=
XM_011545851.2:c.235C=	XP_011544153.1:p.Gln79=
XM_017023216.1:c.235C=	XP_016878705.1:p.Gln79=
NM_000632.4:c.235C= MANE Select	NP_000623.2:p.Gln79=
NM_001145808.2:c.235C=	NP_001139280.1:p.Gln79=