Canonical Allele Identifier: CA494707325

Gene: ITGAM

Linked Data

• MyVariant Identifiers: chr16:g.31276776G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265455G>A , CM000678.2:g.31265455G>A	GRCh38
NC_000016.9:g.31276776G>A , CM000678.1:g.31276776G>A	GRCh37
NC_000016.8:g.31184277G>A	NCBI36
NG_011719.1:g.10489G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.195G>A MANE Select	ENSP00000441691.3:p.Gln65=
ENST00000648685.1:c.195G>A	ENSP00000496959.1:p.Gln65=
ENST00000287497.12:c.195G>A	ENSP00000287497.8:p.Gln65=
ENST00000544665.7:c.195G>A	ENSP00000441691.2:p.Gln65=
NM_000632.3:c.195G>A	NP_000623.2:p.Gln65=
NM_001145808.1:c.195G>A	NP_001139280.1:p.Gln65=
XM_006721045.1:c.195G>A	XP_006721108.1:p.Gln65=
XM_011545850.1:c.-21G>A	XP_011544152.1:n.-21G>A
XM_011545851.1:c.195G>A	XP_011544153.1:p.Gln65=
XR_950796.1:n.285G>A
XM_011545850.2:c.-21G>A	XP_011544152.1:n.-21G>A
XM_011545851.2:c.195G>A	XP_011544153.1:p.Gln65=
XM_017023216.1:c.195G>A	XP_016878705.1:p.Gln65=
NM_000632.4:c.195G>A MANE Select	NP_000623.2:p.Gln65=
NM_001145808.2:c.195G>A	NP_001139280.1:p.Gln65=