Canonical Allele Identifier: CA2216992435

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265648_31265649delinsAT , CM000678.2:g.31265648_31265649delinsAT	GRCh38
NC_000016.9:g.31276969_31276970delinsAT , CM000678.1:g.31276969_31276970delinsAT	GRCh37
NC_000016.8:g.31184470_31184471delinsAT	NCBI36
NG_011719.1:g.10682_10683delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.238+150_238+151delinsAT MANE Select	ENSP00000441691.3:n.238+150_238+151delinsAT
ENST00000648685.1:c.238+150_238+151delinsAT	ENSP00000496959.1:n.238+150_238+151delinsAT
ENST00000287497.12:c.238+150_238+151delinsAT	ENSP00000287497.8:n.238+150_238+151delinsAT
ENST00000544665.7:c.238+150_238+151delinsAT	ENSP00000441691.2:n.238+150_238+151delinsAT
NM_000632.3:c.238+150_238+151delinsAT	NP_000623.2:n.238+150_238+151delinsAT
NM_001145808.1:c.238+150_238+151delinsAT	NP_001139280.1:n.238+150_238+151delinsAT
XM_006721045.1:c.238+150_238+151delinsAT	XP_006721108.1:n.238+150_238+151delinsAT
XM_011545850.1:c.24-134_24-133delinsAT	XP_011544152.1:n.24-134_24-133delinsAT
XM_011545851.1:c.238+150_238+151delinsAT	XP_011544153.1:n.238+150_238+151delinsAT
XR_950796.1:n.328+150_328+151delinsAT
XM_011545850.2:c.24-134_24-133delinsAT	XP_011544152.1:n.24-134_24-133delinsAT
XM_011545851.2:c.238+150_238+151delinsAT	XP_011544153.1:n.238+150_238+151delinsAT
XM_017023216.1:c.238+150_238+151delinsAT	XP_016878705.1:n.238+150_238+151delinsAT
NM_000632.4:c.238+150_238+151delinsAT MANE Select	NP_000623.2:n.238+150_238+151delinsAT
NM_001145808.2:c.238+150_238+151delinsAT	NP_001139280.1:n.238+150_238+151delinsAT