Canonical Allele Identifier: CA2216992200

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265505C= , CM000678.2:g.31265505C=	GRCh38
NC_000016.9:g.31276826C= , CM000678.1:g.31276826C=	GRCh37
NC_000016.8:g.31184327C=	NCBI36
NG_011719.1:g.10539C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.238+7C= MANE Select	ENSP00000441691.3:n.238+7C=
ENST00000648685.1:c.238+7C=	ENSP00000496959.1:n.238+7C=
ENST00000287497.12:c.238+7C=	ENSP00000287497.8:n.238+7C=
ENST00000544665.7:c.238+7C=	ENSP00000441691.2:n.238+7C=
NM_000632.3:c.238+7C=	NP_000623.2:n.238+7C=
NM_001145808.1:c.238+7C=	NP_001139280.1:n.238+7C=
XM_006721045.1:c.238+7C=	XP_006721108.1:n.238+7C=
XM_011545850.1:c.23+7C=	XP_011544152.1:n.23+7C=
XM_011545851.1:c.238+7C=	XP_011544153.1:n.238+7C=
XR_950796.1:n.328+7C=
XM_011545850.2:c.23+7C=	XP_011544152.1:n.23+7C=
XM_011545851.2:c.238+7C=	XP_011544153.1:n.238+7C=
XM_017023216.1:c.238+7C=	XP_016878705.1:n.238+7C=
NM_000632.4:c.238+7C= MANE Select	NP_000623.2:n.238+7C=
NM_001145808.2:c.238+7C=	NP_001139280.1:n.238+7C=