Canonical Allele Identifier: CA2216980432

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31301970T= , CM000678.2:g.31301970T=	GRCh38
NC_000016.9:g.31313291T= , CM000678.1:g.31313291T=	GRCh37
NC_000016.8:g.31220792T=	NCBI36
NG_011719.1:g.47004T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.1707+4016T= MANE Select	ENSP00000441691.3:n.1707+4016T=
ENST00000648685.1:c.1710+4016T=	ENSP00000496959.1:n.1710+4016T=
ENST00000287497.12:c.1707+4016T=	ENSP00000287497.8:n.1707+4016T=
ENST00000544665.7:c.1710+4016T=	ENSP00000441691.2:n.1710+4016T=
ENST00000567031.1:c.453+4316T=
NM_000632.3:c.1707+4016T=	NP_000623.2:n.1707+4016T=
NM_001145808.1:c.1710+4016T=	NP_001139280.1:n.1710+4016T=
XM_006721045.1:c.1707+4016T=	XP_006721108.1:n.1707+4016T=
XM_011545850.1:c.1524+4016T=	XP_011544152.1:n.1524+4016T=
XM_011545851.1:c.1710+4016T=	XP_011544153.1:n.1710+4016T=
XR_950796.1:n.1800+4016T=
XM_011545850.2:c.1524+4016T=	XP_011544152.1:n.1524+4016T=
XM_011545851.2:c.1710+4016T=	XP_011544153.1:n.1710+4016T=
XM_017023216.1:c.1710+4016T=	XP_016878705.1:n.1710+4016T=
NM_000632.4:c.1707+4016T= MANE Select	NP_000623.2:n.1707+4016T=
NM_001145808.2:c.1710+4016T=	NP_001139280.1:n.1710+4016T=