Canonical Allele Identifier: CA8025152

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265490G>A , CM000678.2:g.31265490G>A	GRCh38
NC_000016.9:g.31276811G>A , CM000678.1:g.31276811G>A	GRCh37
NC_000016.8:g.31184312G>A	NCBI36
NG_011719.1:g.10524G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000632.4:c.230G>A MANE Select	NP_000623.2:p.Arg77His
ENST00000544665.9:c.230G>A MANE Select	ENSP00000441691.3:p.Arg77His
NM_000632.3:c.230G>A	NP_000623.2:p.Arg77His
NM_001145808.1:c.230G>A	NP_001139280.1:p.Arg77His
NM_001145808.2:c.230G>A	NP_001139280.1:p.Arg77His
ENST00000287497.12:c.230G>A	ENSP00000287497.8:p.Arg77His
ENST00000544665.7:c.230G>A	ENSP00000441691.2:p.Arg77His
ENST00000648685.1:c.230G>A	ENSP00000496959.1:p.Arg77His
XM_006721045.1:c.230G>A	XP_006721108.1:p.Arg77His
XM_011545850.1:c.15G>A	XP_011544152.1:p.Pro5=
XM_011545850.2:c.15G>A	XP_011544152.1:p.Pro5=
XM_011545851.1:c.230G>A	XP_011544153.1:p.Arg77His
XM_011545851.2:c.230G>A	XP_011544153.1:p.Arg77His
XM_017023216.1:c.230G>A	XP_016878705.1:p.Arg77His
XR_950796.1:n.320G>A