Canonical Allele Identifier: CA395682429

Gene: ITGAM

Linked Data

• MyVariant Identifiers: chr16:g.31276721T>A (hg19) ; chr16:g.31265400T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265400T>A , CM000678.2:g.31265400T>A	GRCh38
NC_000016.9:g.31276721T>A , CM000678.1:g.31276721T>A	GRCh37
NC_000016.8:g.31184222T>A	NCBI36
NG_011719.1:g.10434T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000544665.9:c.140T>A MANE Select	ENSP00000441691.3:p.Val47Glu
ENST00000648685.1:c.140T>A	ENSP00000496959.1:p.Val47Glu
ENST00000287497.12:c.140T>A	ENSP00000287497.8:p.Val47Glu
ENST00000544665.7:c.140T>A	ENSP00000441691.2:p.Val47Glu
NM_000632.3:c.140T>A	NP_000623.2:p.Val47Glu
NM_001145808.1:c.140T>A	NP_001139280.1:p.Val47Glu
XM_006721045.1:c.140T>A	XP_006721108.1:p.Val47Glu
XM_011545850.1:c.-76T>A	XP_011544152.1:n.-76T>A
XM_011545851.1:c.140T>A	XP_011544153.1:p.Val47Glu
XR_950796.1:n.230T>A
XM_011545850.2:c.-76T>A	XP_011544152.1:n.-76T>A
XM_011545851.2:c.140T>A	XP_011544153.1:p.Val47Glu
XM_017023216.1:c.140T>A	XP_016878705.1:p.Val47Glu
NM_000632.4:c.140T>A MANE Select	NP_000623.2:p.Val47Glu
NM_001145808.2:c.140T>A	NP_001139280.1:p.Val47Glu