Canonical Allele Identifier: CA2216992343

Gene: ITGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31265589_31265590delinsTG , CM000678.2:g.31265589_31265590delinsTG	GRCh38
NC_000016.9:g.31276910_31276911delinsTG , CM000678.1:g.31276910_31276911delinsTG	GRCh37
NC_000016.8:g.31184411_31184412delinsTG	NCBI36
NG_011719.1:g.10623_10624delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544665.9:c.238+91_238+92delinsTG MANE Select	ENSP00000441691.3:n.238+91_238+92delinsTG
ENST00000648685.1:c.238+91_238+92delinsTG	ENSP00000496959.1:n.238+91_238+92delinsTG
ENST00000287497.12:c.238+91_238+92delinsTG	ENSP00000287497.8:n.238+91_238+92delinsTG
ENST00000544665.7:c.238+91_238+92delinsTG	ENSP00000441691.2:n.238+91_238+92delinsTG
NM_000632.3:c.238+91_238+92delinsTG	NP_000623.2:n.238+91_238+92delinsTG
NM_001145808.1:c.238+91_238+92delinsTG	NP_001139280.1:n.238+91_238+92delinsTG
XM_006721045.1:c.238+91_238+92delinsTG	XP_006721108.1:n.238+91_238+92delinsTG
XM_011545850.1:c.23+91_23+92delinsTG	XP_011544152.1:n.23+91_23+92delinsTG
XM_011545851.1:c.238+91_238+92delinsTG	XP_011544153.1:n.238+91_238+92delinsTG
XR_950796.1:n.328+91_328+92delinsTG
XM_011545850.2:c.23+91_23+92delinsTG	XP_011544152.1:n.23+91_23+92delinsTG
XM_011545851.2:c.238+91_238+92delinsTG	XP_011544153.1:n.238+91_238+92delinsTG
XM_017023216.1:c.238+91_238+92delinsTG	XP_016878705.1:n.238+91_238+92delinsTG
NM_000632.4:c.238+91_238+92delinsTG MANE Select	NP_000623.2:n.238+91_238+92delinsTG
NM_001145808.2:c.238+91_238+92delinsTG	NP_001139280.1:n.238+91_238+92delinsTG