Canonical Allele Identifier: CA395682402

Gene: ITGAM

Linked Data

• MyVariant Identifiers: chr16:g.31276718T>C (hg19) ; chr16:g.31265397T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265397T>C , CM000678.2:g.31265397T>C	GRCh38
NC_000016.9:g.31276718T>C , CM000678.1:g.31276718T>C	GRCh37
NC_000016.8:g.31184219T>C	NCBI36
NG_011719.1:g.10431T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.137T>C MANE Select	ENSP00000441691.3:p.Val46Ala
ENST00000648685.1:c.137T>C	ENSP00000496959.1:p.Val46Ala
ENST00000287497.12:c.137T>C	ENSP00000287497.8:p.Val46Ala
ENST00000544665.7:c.137T>C	ENSP00000441691.2:p.Val46Ala
NM_000632.3:c.137T>C	NP_000623.2:p.Val46Ala
NM_001145808.1:c.137T>C	NP_001139280.1:p.Val46Ala
XM_006721045.1:c.137T>C	XP_006721108.1:p.Val46Ala
XM_011545850.1:c.-79T>C	XP_011544152.1:n.-79T>C
XM_011545851.1:c.137T>C	XP_011544153.1:p.Val46Ala
XR_950796.1:n.227T>C
XM_011545850.2:c.-79T>C	XP_011544152.1:n.-79T>C
XM_011545851.2:c.137T>C	XP_011544153.1:p.Val46Ala
XM_017023216.1:c.137T>C	XP_016878705.1:p.Val46Ala
NM_000632.4:c.137T>C MANE Select	NP_000623.2:p.Val46Ala
NM_001145808.2:c.137T>C	NP_001139280.1:p.Val46Ala