Canonical Allele Identifier: CA8025909

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31326926A>G , CM000678.2:g.31326926A>G	GRCh38
NC_000016.9:g.31338247A>G , CM000678.1:g.31338247A>G	GRCh37
NC_000016.8:g.31245748A>G	NCBI36
NG_011719.1:g.71960A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000632.4:c.2699A>G MANE Select	NP_000623.2:p.Asn900Ser
ENST00000544665.9:c.2699A>G MANE Select	ENSP00000441691.3:p.Asn900Ser
NM_000632.3:c.2699A>G	NP_000623.2:p.Asn900Ser
NM_001145808.1:c.2702A>G	NP_001139280.1:p.Asn901Ser
NM_001145808.2:c.2702A>G	NP_001139280.1:p.Asn901Ser
ENST00000287497.12:c.2699A>G	ENSP00000287497.8:p.Asn900Ser
ENST00000544665.7:c.2702A>G	ENSP00000441691.2:p.Asn901Ser
ENST00000561838.1:n.515A>G
ENST00000648685.1:c.2702A>G	ENSP00000496959.1:p.Asn901Ser
XM_011545850.1:c.2516A>G	XP_011544152.1:p.Asn839Ser
XM_011545850.2:c.2516A>G	XP_011544152.1:p.Asn839Ser
XM_017023216.1:c.2702A>G	XP_016878705.1:p.Asn901Ser
XR_950796.1:n.2792A>G